Canonical Allele Identifier: PA2825143389
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1073478
ClinVar RCV Id: RCV001386500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Met581Lys
CA281504517
NM_000339.3:c.1742T>A