Allele Registry

Canonical Allele Identifier: PA2827281535

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000559680

RCV000851194

ClinVar Variation:

478110

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.His245Tyr	CA355753773 NM_001329964.2:c.733C>T