Canonical Allele Identifier: PA2826601538
Gene: CLCN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 591443
ClinVar RCV Id: RCV000722622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269092.1:p.Asp411Ala
CA413185937
NM_001282163.2:c.1232A>C