Canonical Allele Identifier: PA2580110961
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072072
ClinVar RCV Id: RCV002949474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Met881Val
CA8069982
NM_000339.3:c.2641A>G