Canonical Allele Identifier: PA2825595673
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Arg208Trp
CA119768
NM_001126107.2:c.622C>T