Canonical Allele Identifier: PA2826077419
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800219
ClinVar RCV Id: RCV000983885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164559.1:p.Leu396Phe
CA2734173
NM_001171088.2:c.1186C>T