Canonical Allele Identifier: PA916006550
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 389644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe70Val
CA16608667
NM_001276761.3:c.208T>G