Canonical Allele Identifier: PA2826880635
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060918
ClinVar RCV Id: RCV001370417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290179.1:p.Ile327_Ter328insSerAspLeuGlySerPheThrGlu
CA360698000
NM_001303250.3:c.983G>C