Canonical Allele Identifier: PA169126
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Asp7His
CA000065
NM_000546.6:c.19G>C