Canonical Allele Identifier: PA2827265496
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Arg172Gln
CA118348
NM_001329149.2:c.515G>A