Canonical Allele Identifier: PA2825782551
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407513
ClinVar RCV Id: RCV001937808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Gly1020Arg
CA409207784
NM_001134771.2:c.3058G>A
CA409207785
NM_001134771.2:c.3058G>C