Canonical Allele Identifier: PA2827265532
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Arg224His
CA118339
NM_001329149.2:c.671G>A