Allele Registry

Canonical Allele Identifier: PA2826077032

Gene: CLCN2 HGNC NCBI

ClinVar RCV:

RCV000201825

RCV001511096

ClinVar Variation:

217776

HGVS (amino-acid)	Matching Registered Transcripts
NP_001164558.1:p.Thr651Ser	CA347638 NM_001171087.2:c.1952C>G CA355448820 NM_001171087.2:c.1951A>T