Canonical Allele Identifier: PA107082
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Leu252Pro
CA000398
NM_000546.6:c.755T>C