Allele Registry

Canonical Allele Identifier: PA2826148811

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV003509947

ClinVar Variation:

2752676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Tyr458Asn	CA414002868 NM_001184880.2:c.1372T>A