Canonical Allele Identifier: PA915977820
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 523358
ClinVar RCV Id: RCV000626664 RCV001860477 RCV002289914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Val153Met
CA8069044
NM_001126108.2:c.457G>A