Canonical Allele Identifier: PA2825596077
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 319903
ClinVar RCV Id: RCV000286818 RCV000414425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Gly462Arg
CA8069451
NM_001126107.2:c.1384G>A
CA395987538
NM_001126107.2:c.1384G>C