Allele Registry

Canonical Allele Identifier: PA2826077629

Gene: CLCN2 HGNC NCBI

ClinVar RCV:

RCV000201825

RCV001511096

ClinVar Variation:

217776

HGVS (amino-acid)	Matching Registered Transcripts
NP_001164559.1:p.Thr624Ser	CA347638 NM_001171088.2:c.1871C>G CA355448820 NM_001171088.2:c.1870A>T