Canonical Allele Identifier: PA2579954649
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro27Thr
CA16615735
NM_000546.6:c.79C>A