Canonical Allele Identifier: PA2826562641
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 666137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ala148Val
CA397836165
NM_001276697.3:c.443C>T