Canonical Allele Identifier: PA174180
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 161514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Arg132His
CA174179
NM_001114980.1:c.395G>A