Allele Registry

Canonical Allele Identifier: PA2741966823

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV003509947

ClinVar Variation:

2752676

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Tyr458Asn	CA414002868 NM_020766.3:c.1372T>A