Canonical Allele Identifier: PA107198
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro152Leu
CA000204
NM_000546.6:c.455C>T
CA645589087
NM_000546.6:c.454_455delinsTT