Canonical Allele Identifier: PA2825596039
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536259
ClinVar RCV Id: RCV003266200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Thr430Ser
CA8069415
NM_001126107.2:c.1289C>G
CA395986152
NM_001126107.2:c.1288A>T