Allele Registry

Canonical Allele Identifier: PA2826148541

Gene: PCDH19 HGNC NCBI

ClinVar RCV:

RCV001211167

ClinVar Variation:

941388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171809.1:p.Thr146Lys	CA414009704 NM_001184880.2:c.437C>A