Allele Registry

Canonical Allele Identifier: PA316338

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188364

RCV000698779

ClinVar Variation:

206327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Arg372Trp	CA316336 NM_001184880.2:c.1114C>T