Canonical Allele Identifier: PA107099
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 245777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Leu265Pro
CA10584586
NM_000546.6:c.794T>C
CA645588450
NM_000546.6:c.794_795delinsCT