Canonical Allele Identifier: PA2825580609
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2855280
ClinVar RCV Id: RCV003757781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108453.1:p.Asn152Asp
CA355753762
NM_001114981.1:c.454A>G