Canonical Allele Identifier: PA915978121
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 319922
ClinVar RCV Id: RCV000261759 RCV002522874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Thr996Asn
CA8070182
NM_001126108.2:c.2987C>A