Allele Registry

Canonical Allele Identifier: PA2825579723

Gene: TP63 HGNC NCBI

ClinVar Allele:

204641

ClinVar RCV:

RCV000190455

ClinVar Variation:

208418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108450.1:p.Ala346Gly	CA204448 NM_001114978.2:c.1037C>G