Canonical Allele Identifier: PA106599
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg158His
CA000227
NM_000546.6:c.473G>A