Canonical Allele Identifier: PA915977887
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 209191
ClinVar RCV Id: RCV000191129 RCV000681951
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Leu272Pro
CA250393
NM_001126108.2:c.815T>C