Canonical Allele Identifier: PA169588
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro72Ala
CA000070
NM_000546.6:c.214C>G