Allele Registry

Canonical Allele Identifier: PA2827265554

Gene: TP63 HGNC NCBI

ClinVar Allele:

204641

ClinVar RCV:

RCV000190455

ClinVar Variation:

208418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316078.1:p.Ala252Gly	CA204448 NM_001329149.2:c.755C>G