Canonical Allele Identifier: PA915986049
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 92110
ClinVar RCV Id: RCV000077782 RCV000292034 RCV000404137 RCV001854367 RCV003474671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Arg356Gln
CA266749
NM_001160210.2:c.1067G>A