Allele Registry

Canonical Allele Identifier: PA2825553156

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000489751

ClinVar Variation:

427126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098713.1:p.Asp121Asn	CA414010340 NM_001105243.2:c.361G>A