Canonical Allele Identifier: PA2827281579
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg316His
CA118339
NM_001329964.2:c.947G>A