Allele Registry

Canonical Allele Identifier: PA916049899

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188345

ClinVar Variation:

206309

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp121His	CA316284 NM_020766.3:c.361G>C