Allele Registry

Canonical Allele Identifier: PA916049882

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000485618

ClinVar Variation:

421597

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Cys99Ser	CA16621150 NM_020766.3:c.295T>A CA414010804 NM_020766.3:c.296G>C