Allele Registry

Canonical Allele Identifier: PA1139730634

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001041816

RCV001257661

ClinVar Variation:

839943

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp264His	CA414008109 NM_020766.3:c.790G>C