Canonical Allele Identifier: PA2826564305
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376678
ClinVar RCV Id: RCV000418040 RCV000420871 RCV000422877 RCV000422166 RCV000428087 RCV000428696 RCV000429377 RCV000433566 RCV000435261 RCV000440106 RCV000439367 RCV000701251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Val115Leu
CA16603092
NM_001276699.3:c.343G>C