Canonical Allele Identifier: PA2825052348
Gene: CLCNKB HGNC NCBI

Linked Data

ClinVar Variation Id: 2096568
ClinVar RCV Id: RCV003028245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000076.2:p.Val570_Lys578dup
CA623984
NM_000085.5:c.1708_1734dup