Allele Registry

Canonical Allele Identifier: PA916027708

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV003593293

ClinVar Variation:

2734605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316078.1:p.Gly79Asp	CA343283 NM_001329149.2:c.236G>A