Canonical Allele Identifier: PA2825142972
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Arg209Trp
CA119768
NM_000339.3:c.625C>T