Canonical Allele Identifier: PA915986082
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 361014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153682.1:p.Gly466Cys
CA4352941
NM_001160210.2:c.1396G>T