Canonical Allele Identifier: PA915986064
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 361022
ClinVar RCV Id: RCV000292722 RCV000350029 RCV002519511 RCV001095144 RCV001272331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Gly364Val
CA4353038
NM_001160210.2:c.1091G>T