Canonical Allele Identifier: PA2825596524
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 208612
ClinVar RCV Id: RCV000190624 RCV000255367 RCV000626663 RCV001328096 RCV003401040 RCV004017477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119579.2:p.Gly740Arg
CA204579
NM_001126107.2:c.2218G>A
CA395994702
NM_001126107.2:c.2218G>C