Canonical Allele Identifier: PA2825595900
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Pro348Leu
CA119776
NM_001126107.2:c.1043C>T