Allele Registry

Canonical Allele Identifier: PA916049907

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000079608

RCV001064429

ClinVar Variation:

93676

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asn125Ser	CA221632 NM_020766.3:c.374A>G