Canonical Allele Identifier: PA2829948457
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 653443
ClinVar RCV Id: RCV000809219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Asp962Gly
CA409207480
NM_020708.5:c.2885A>G