Allele Registry

Canonical Allele Identifier: PA2825553088

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000485018

ClinVar Variation:

422522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Glu31Val	CA16621152 NM_001105243.2:c.92A>T