Allele Registry

Canonical Allele Identifier: PA916050032

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000147085

RCV000490161

ClinVar Variation:

159562

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp264Tyr	CA172968 NM_020766.3:c.790G>T