ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563134
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376612
ClinVar RCV Id:
RCV000417520
RCV000418213
RCV000422374
RCV000422912
RCV000423516
RCV000424851
RCV000429577
RCV000427668
RCV000428197
RCV000428877
RCV000434205
RCV000433585
RCV000434933
RCV000435420
RCV000435566
RCV000440128
RCV000439568
RCV000442541
RCV000444985
RCV000445292
RCV000991151
RCV001525967
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.His34Pro
CA16603033
NM_001276698.3:c.101A>C