Allele Registry

Canonical Allele Identifier: PA1139730461

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001211167

ClinVar Variation:

941388

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Thr146Lys	CA414009704 NM_020766.3:c.437C>A