Canonical Allele Identifier: PA2825598130
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736354
ClinVar RCV Id: RCV003559919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Leu849Phe
CA395997319
NM_001126108.2:c.2545C>T