ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826561410
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376652
ClinVar RCV Id:
RCV000417693
RCV000418362
RCV000420498
RCV000422668
RCV000423297
RCV000425782
RCV000424776
RCV000425100
RCV000425394
RCV000427544
RCV000427948
RCV000430735
RCV000432931
RCV000432207
RCV000433611
RCV000435353
RCV000435050
RCV000436038
RCV000437882
RCV000441010
RCV000441711
RCV000440334
RCV000444356
RCV000444519
RCV000444427
RCV000633396
RCV000626118
RCV001026425
RCV004022238
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Arg209Gly
CA16603069
NM_001276696.3:c.625C>G