Allele Registry

Canonical Allele Identifier: PA916050148

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000485418

ClinVar Variation:

420879

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Tyr458His	CA16621148 NM_020766.3:c.1372T>C