Allele Registry

Canonical Allele Identifier: PA316375

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188377

RCV001297616

ClinVar Variation:

206340

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Arg625Gly	CA316374 NM_001105243.2:c.1873A>G