Allele Registry

Canonical Allele Identifier: PA121294

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000011763

ClinVar Variation:

11016

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Val441Glu	CA121293 NM_020766.3:c.1322T>A