Canonical Allele Identifier: PA2826561962
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ser24Leu
CA397841206
NM_001276697.3:c.71C>T