Canonical Allele Identifier: PA2825579997
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.His247Arg
CA339766
NM_001114979.2:c.740A>G