Canonical Allele Identifier: PA2580103488
Gene: CLCNKB HGNC NCBI

Linked Data

ClinVar Variation Id: 2429674
ClinVar RCV Id: RCV003127128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000076.2:p.Ala204Val
CA338635291
NM_000085.5:c.611C>T