Allele Registry

Canonical Allele Identifier: PA916049988

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188358

RCV001379622

ClinVar Variation:

206322

1068161

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asn232Lys	CA316321 NM_020766.3:c.696T>A CA414008610 NM_020766.3:c.696T>G