Canonical Allele Identifier: PA2827281514
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 161514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg224His
CA174179
NM_001329964.2:c.671G>A