Allele Registry

Canonical Allele Identifier: PA916049927

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188350

ClinVar Variation:

206314

HGVS (amino-acid)	Matching Registered Transcripts
NP_065817.2:p.Asp155Asn	CA316298 NM_020766.3:c.463G>A