Allele Registry

Canonical Allele Identifier: PA2827281478

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV003593293

ClinVar Variation:

2734605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.Gly171Asp	CA343283 NM_001329964.2:c.512G>A