Allele Registry

Canonical Allele Identifier: PA645485745

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000485018

ClinVar Variation:

422522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Glu31Val	CA16621152 NM_001184880.2:c.92A>T