Canonical Allele Identifier: PA294066
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Thr312Ser
CA000505
NM_000546.6:c.935C>G
CA397836079
NM_000546.6:c.934A>T