Canonical Allele Identifier: PA2825598167
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303037
ClinVar Variation Id: 2961051
ClinVar RCV Id: RCV003819762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Gly867Ser
CA8069978
NM_001126108.2:c.2599G>A
CA2740093387
NM_001126108.2:c.2598_2599delinsTA