Canonical Allele Identifier: PA2579936882
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 823709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Phe113Ser
CA397844504
NM_000546.6:c.338T>C