Allele Registry

Canonical Allele Identifier: PA109694

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188357

RCV000641136

RCV002317136

ClinVar Variation:

206321

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asn232Ser	CA316319 NM_001184880.2:c.695A>G