Canonical Allele Identifier: PA2825142186
Gene: SLC12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162818
ClinVar RCV Id: RCV004456217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000329.2:p.Gly237Arg
CA392305637
NM_000338.3:c.709G>A
CA392305639
NM_000338.3:c.709G>C