Canonical Allele Identifier: PA2825946387
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 594933
ClinVar RCV Id: RCV000730338 RCV001244437 RCV001830607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Arg292Trp
CA4353113
NM_001160210.2:c.874C>T