Canonical Allele Identifier: PA2579935329
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val217Leu
CA397839964
NM_000546.6:c.649G>C
CA397839966
NM_000546.6:c.649G>T