Canonical Allele Identifier: PA2826077386
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3145398
ClinVar RCV Id: RCV004444239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164559.1:p.Pro337Arg
CA2734220
NM_001171088.2:c.1010C>G