Canonical Allele Identifier: PA2825649317
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394394
ClinVar RCV Id: RCV001900894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg294Gly
CA338441713
NM_001127660.2:c.880C>G