Allele Registry

Canonical Allele Identifier: PA916049842

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000700933

ClinVar Variation:

578043

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Glu31Lys	CA414011397 NM_020766.3:c.91G>A