Canonical Allele Identifier: PA891858501
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 583282
ClinVar RCV Id: RCV000707575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620128.1:p.Ile405Val
CA360697829
NM_138773.4:c.1213A>G