Canonical Allele Identifier: PA2826567569
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 496049
ClinVar RCV Id: RCV000588420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu250Val
CA397836620
NM_001276761.3:c.748C>G