Canonical Allele Identifier: PA2573181939
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499809
ClinVar RCV Id: RCV002013053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Thr972Met
CA9887720
NM_001134771.2:c.2915C>T