Canonical Allele Identifier: PA2825142953
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2281747
ClinVar RCV Id: RCV002848590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Thr180Ser
CA395980911
NM_000339.3:c.538A>T