Canonical Allele Identifier: PA915977772
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 505768
ClinVar RCV Id: RCV000607947 RCV000681735 RCV000778470 RCV002529351 RCV003424170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Glu121Asp
CA8068995
NM_001126108.2:c.363G>C
CA395978914
NM_001126108.2:c.363G>T