Canonical Allele Identifier: PA2573190302
Gene: CLCN7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505201
ClinVar RCV Id: RCV002020425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278.1:p.Arg756Trp
CA7809862
NM_001287.6:c.2266C>T