Canonical Allele Identifier: PA2825571105
Gene: CLCN7 HGNC NCBI

Linked Data

ClinVar Variation Id: 65635
ClinVar RCV Id: RCV001843355 RCV001781390 RCV003415823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107803.1:p.Gly191Arg
CA344955
NM_001114331.3:c.571G>A
CA394191921
NM_001114331.3:c.571G>C