Canonical Allele Identifier: PA658679199
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala88Val
CA397845305
NM_001126114.3:c.263C>T