Canonical Allele Identifier: PA2826561732
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 666137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ala268Val
CA397836165
NM_001276696.3:c.803C>T