Canonical Allele Identifier: PA2825649322
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 199133
ClinVar RCV Id: RCV000180646 RCV000321170 RCV000205710 RCV000986246 RCV000658493 RCV001172690 RCV002492791 RCV002444723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Gly298Arg
CA303079
NM_001127660.2:c.892G>A
CA18010015
NM_001127660.2:c.892G>C