Canonical Allele Identifier: PA2826395242
Gene: SLC12A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373721
ClinVar RCV Id: RCV001900438 RCV002482589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243390.1:p.Leu1192Val
CA3393744
NM_001256461.2:c.3574C>G