Canonical Allele Identifier: PA2573173140
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_001037.1:p.Leu1208Val
CA3393744
NM_001046.3:c.3622C>G