Allele Registry

Canonical Allele Identifier: PA916050083

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188364

RCV000698779

ClinVar Variation:

206327

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Arg372Trp	CA316336 NM_020766.3:c.1114C>T