Canonical Allele Identifier: PA2825598136
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490589
ClinVar RCV Id: RCV001983815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Leu850Phe
CA395997333
NM_001126108.2:c.2548C>T