Allele Registry

Canonical Allele Identifier: PA916050076

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000802161

RCV002249515

ClinVar Variation:

647613

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Pro344Gln	CA414004648 NM_020766.3:c.1031C>A