Allele Registry

Canonical Allele Identifier: PA2825553098

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000478041

ClinVar Variation:

422031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Ala43Val	CA16621151 NM_001105243.2:c.128C>T