Canonical Allele Identifier: PA2579935298
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro222Ser
CA16615720
NM_000546.6:c.664C>T