Canonical Allele Identifier: PA2825409900
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2160331
ClinVar RCV Id: RCV003075894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035962.1:p.Gly93Arg
CA7464591
NM_001042497.2:c.277G>A
CA391614848
NM_001042497.2:c.277G>C