Canonical Allele Identifier: PA2826078084
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079677
ClinVar RCV Id: RCV002998703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164560.1:p.Arg408Cys
CA355452673
NM_001171089.2:c.1222C>T