Canonical Allele Identifier: PA264216
Gene: CLCN7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56890
ClinVar RCV Id: RCV000050235 RCV000055847 RCV000480176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278.1:p.Tyr99Cys
CA264215
NM_001287.6:c.296A>G