Canonical Allele Identifier: PA916076563
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 644671
ClinVar RCV Id: RCV000798640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Ala979Thr
CA9887755
NM_020708.5:c.2935G>A