Canonical Allele Identifier: PA2825580617
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108453.1:p.Arg172Gln
CA118348
NM_001114981.1:c.515G>A