Canonical Allele Identifier: PA2826007960
Gene: CLCNKB HGNC NCBI

Linked Data

ClinVar Variation Id: 447094
ClinVar RCV Id: RCV000516781 RCV001579038 RCV001579039 RCV001683550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159417.2:p.Met393Thr
CA623979
NM_001165945.2:c.1178T>C