Canonical Allele Identifier: PA2580103483
Gene: CLCNKB HGNC NCBI

Linked Data

ClinVar Variation Id: 2151864
ClinVar RCV Id: RCV003078999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000076.2:p.Met176Ile
CA623358
NM_000085.5:c.528G>C
CA338634907
NM_000085.5:c.528G>A
CA338634910
NM_000085.5:c.528G>T