Canonical Allele Identifier: PA2825579717
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Arg343Gln
CA118340
NM_001114978.2:c.1028G>A