Canonical Allele Identifier: PA2825143218
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536259
ClinVar RCV Id: RCV003266200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Thr431Ser
CA8069415
NM_000339.3:c.1292C>G
CA395986152
NM_000339.3:c.1291A>T