Allele Registry

Canonical Allele Identifier: PA916050156

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000479158

RCV002509405

ClinVar Variation:

420880

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp479Asn	CA16621147 NM_020766.3:c.1435G>A