Allele Registry

Canonical Allele Identifier: PA316318

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV000188356

ClinVar Variation:

206320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Asp212His	CA316316 NM_001184880.2:c.634G>C