Canonical Allele Identifier: PA2826880630
Gene: SLC25A46 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468753
ClinVar RCV Id: RCV001970732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290179.1:p.Asn325Thr
CA360697958
NM_001303250.3:c.974A>C