Canonical Allele Identifier: PA2825579988
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.Arg243Gln
CA118335
NM_001114979.2:c.728G>A