Canonical Allele Identifier: PA915977965
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 319903
ClinVar RCV Id: RCV000286818 RCV000414425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Gly463Arg
CA8069451
NM_001126108.2:c.1387G>A
CA395987538
NM_001126108.2:c.1387G>C