Allele Registry

Canonical Allele Identifier: PA916049900

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000489751

ClinVar Variation:

427126

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp121Asn	CA414010340 NM_020766.3:c.361G>A