Canonical Allele Identifier: PA2825580215
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716376
ClinVar RCV Id: RCV002304670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Cys150Arg
CA355753740
NM_001114980.1:c.448T>C