Canonical Allele Identifier: PA2825143490
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 8589
ClinVar RCV Id: RCV000009120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Arg655Leu
CA119772
NM_000339.3:c.1964G>T