ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826561557
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12366
ClinVar RCV Id:
RCV000013163
RCV000013164
RCV000115738
RCV000254693
RCV000418930
RCV000424109
RCV000422097
RCV000424627
RCV000422733
RCV000424218
RCV000431361
RCV000434044
RCV000436207
RCV000441169
RCV000439513
RCV000440815
RCV000443907
RCV000463420
RCV000424833
RCV000428779
RCV000429822
RCV000419960
RCV000433409
RCV000435547
RCV000437210
RCV000423826
RCV000430161
RCV000440474
RCV000444851
RCV000444900
RCV000785345
RCV001358389
RCV001527484
RCV001257517
RCV001527470
RCV002476955
RCV003162246
RCV003466853
RCV003492292
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Arg234His
CA000434
NM_001276696.3:c.701G>A