Canonical Allele Identifier: PA2825580427
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 650415
ClinVar RCV Id: RCV000805566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Phe471Val
CA355759033
NM_001114980.1:c.1411T>G