Canonical Allele Identifier: PA2826880484
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 1746002
ClinVar RCV Id: RCV002338594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290178.1:p.His318Arg
CA360697746
NM_001303249.3:c.953A>G