Allele Registry

Canonical Allele Identifier: PA645485787

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000485618

ClinVar Variation:

421597

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Cys99Ser	CA16621150 NM_001184880.2:c.295T>A CA414010804 NM_001184880.2:c.296G>C