Canonical Allele Identifier: PA2579954652
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro27Ser
CA287489277
NM_000546.6:c.79C>T