Allele Registry

Canonical Allele Identifier: PA2827281480

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000429171

RCV000695697

ClinVar Variation:

383835

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.Gly171Arg	CA16604496 NM_001329964.2:c.511G>C