Canonical Allele Identifier: PA2825142954
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1134717
ClinVar RCV Id: RCV001469740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Thr180Met
CA8069092
NM_000339.3:c.539C>T