Canonical Allele Identifier: PA2825596849
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1077594
ClinVar RCV Id: RCV001392216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Thr955Met
CA8070071
NM_001126107.2:c.2864C>T