Canonical Allele Identifier: PA2825142876
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 505768
ClinVar RCV Id: RCV000607947 RCV000681735 RCV000778470 RCV002529351 RCV003424170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Glu121Asp
CA8068995
NM_000339.3:c.363G>C
CA395978914
NM_000339.3:c.363G>T