Canonical Allele Identifier: PA915977891
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_001119580.2:p.Ala322Val
CA8069291
NM_001126108.2:c.965C>T