Canonical Allele Identifier: PA2826880339
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 475792
ClinVar RCV Id: RCV000538515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290178.1:p.Val66Leu
CA360693342
NM_001303249.3:c.196G>C
CA360693343
NM_001303249.3:c.196G>T