Canonical Allele Identifier: PA915961033
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 487479
ClinVar RCV Id: RCV000576426 RCV002526929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Asp841Gly
CA395996336
NM_000339.3:c.2522A>G