Canonical Allele Identifier: PA658662911
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_000076.2:p.Met562Thr
CA623979
NM_000085.5:c.1685T>C