Allele Registry

Canonical Allele Identifier: PA2827264178

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000429171

RCV000695697

ClinVar Variation:

383835

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316073.1:p.Gly173Arg	CA16604496 NM_001329144.2:c.517G>C