Allele Registry

Canonical Allele Identifier: PA2826989614

Gene: PCDH9 HGNC NCBI

ClinVar RCV:

RCV004119975

ClinVar Variation:

2262685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305302.1:p.Lys1093Glu	CA388357895 NM_001318373.1:c.3277A>G