Canonical Allele Identifier: PA2826601534
Gene: CLCN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081207
ClinVar RCV Id: RCV002979660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269092.1:p.Ser402Gly
CA10413866
NM_001282163.2:c.1204A>G