Allele Registry

Canonical Allele Identifier: PA916049977

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188356

ClinVar Variation:

206320

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp212His	CA316316 NM_020766.3:c.634G>C