Canonical Allele Identifier: PA2580111003
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717373
ClinVar RCV Id: RCV002297565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Gln965Glu
CA396002241
NM_000339.3:c.2893C>G