Canonical Allele Identifier: PA2826880472
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378646
ClinVar RCV Id: RCV001881260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290178.1:p.Met288Ile
CA125344939
NM_001303249.3:c.864G>A
CA360697312
NM_001303249.3:c.864G>C
CA360697317
NM_001303249.3:c.864G>T