Canonical Allele Identifier: PA2826564380
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458571
ClinVar RCV Id: RCV000546011 RCV000563243 RCV001544620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Thr125Ser
CA397836761
NM_001276699.3:c.373A>T