Canonical Allele Identifier: PA354560
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 218665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005126.1:p.Arg32Trp
CA248916
NM_005135.2:c.94C>T