Canonical Allele Identifier: PA2825596726
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 885393
ClinVar RCV Id: RCV001116972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Gln876Arg
CA395997616
NM_001126107.2:c.2627A>G