Allele Registry

Canonical Allele Identifier: PA109920

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188374

RCV002317137

RCV002514027

ClinVar Variation:

206337

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Pro561Arg	CA316366 NM_001184880.2:c.1682C>G