Canonical Allele Identifier: PA2573180039
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497328
ClinVar RCV Id: RCV002019805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Asn442Lys
CA8069421
NM_001126108.2:c.1326C>G
CA395986398
NM_001126108.2:c.1326C>A