Allele Registry

Canonical Allele Identifier: PA347639

Gene: CLCN2 HGNC NCBI

ClinVar RCV:

RCV000201825

RCV001511096

ClinVar Variation:

217776

HGVS (amino-acid)	Matching Registered Transcripts
NP_004357.3:p.Thr668Ser	CA347638 NM_004366.6:c.2003C>G CA355448820 NM_004366.6:c.2002A>T