Canonical Allele Identifier: PA915977876
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 548560
ClinVar RCV Id: RCV000662086 RCV002530592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Ala232Thr
CA8069150
NM_001126108.2:c.694G>A