Canonical Allele Identifier: PA2825579990
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716376
ClinVar RCV Id: RCV002304670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.Cys244Arg
CA355753740
NM_001114979.2:c.730T>C