Allele Registry

Canonical Allele Identifier: PA916049847

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000478041

ClinVar Variation:

422031

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Ala43Val	CA16621151 NM_020766.3:c.128C>T