Canonical Allele Identifier: PA2825596305
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Ala587Val
CA119774
NM_001126107.2:c.1760C>T