Canonical Allele Identifier: PA2825595873
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 498813
ClinVar RCV Id: RCV000591358 RCV000989608 RCV003488715 RCV004024751 RCV003935605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Ala321Val
CA8069291
NM_001126107.2:c.962C>T