Canonical Allele Identifier: PA2826078055
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719668
ClinVar RCV Id: RCV003553719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164560.1:p.Pro381Thr
CA355453513
NM_001171089.2:c.1141C>A