Canonical Allele Identifier: PA915977889
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 448400
ClinVar RCV Id: RCV000516845 RCV001274377 RCV003409740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Ala313Val
CA8069267
NM_001126108.2:c.938C>T