Canonical Allele Identifier: PA2826076848
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2144969
ClinVar RCV Id: RCV003064791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164558.1:p.Pro380Leu
CA2734223
NM_001171087.2:c.1139C>T