Canonical Allele Identifier: PA2825596381
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 267286
ClinVar RCV Id: RCV000576776 RCV003556306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Asn639Ser
CA281505366
NM_001126107.2:c.1916A>G