Canonical Allele Identifier: PA2826147557
Gene: SLC12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716703
ClinVar RCV Id: RCV002295999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171761.1:p.Phe381Ser
CA392308582
NM_001184832.2:c.1142T>C