Canonical Allele Identifier: PA915976696
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 653443
ClinVar RCV Id: RCV000809219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Asp985Gly
CA409207480
NM_001134771.2:c.2954A>G