Canonical Allele Identifier: PA2825596338
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 886419
ClinVar RCV Id: RCV001118613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Lys605Arg
CA395991085
NM_001126107.2:c.1814A>G