Canonical Allele Identifier: PA915953619
Gene: CLCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 638963
ClinVar RCV Id: RCV000791647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000074.3:p.Phe311Cys
CA369641653
NM_000083.3:c.932T>G