Canonical Allele Identifier: PA2579935399
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro219Leu
CA397839907
NM_000546.6:c.656C>T
CA645588728
NM_000546.6:c.656_657delinsTT