Canonical Allele Identifier: PA2825649713
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214648
ClinVar RCV Id: RCV000197786 RCV001101761 RCV001087905 RCV001335680 RCV002415848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg663Cys
CA322248
NM_001127660.2:c.1987C>T