Canonical Allele Identifier: PA2826077401
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442624
ClinVar RCV Id: RCV001953089 RCV002484722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164559.1:p.Thr361Met
CA2734191
NM_001171088.2:c.1082C>T