Canonical Allele Identifier: PA2826880632
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760558
ClinVar RCV Id: RCV002409777 RCV003099742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290179.1:p.Asn326Ser
CA125344945
NM_001303250.3:c.977A>G