Canonical Allele Identifier: PA2825596303
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510058
ClinVar RCV Id: RCV002011478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Trp586Cys
CA395990715
NM_001126107.2:c.1758G>C
CA395990717
NM_001126107.2:c.1758G>T