Allele Registry

Canonical Allele Identifier: PA2826989566

Gene: PCDH9 HGNC NCBI

ClinVar RCV:

RCV004119975

ClinVar Variation:

2262685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305301.1:p.Lys1127Glu	CA388357895 NM_001318372.1:c.3379A>G