Canonical Allele Identifier: PA2825649702
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1495034
ClinVar RCV Id: RCV002015155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu658Asp
CA338451269
NM_001127660.2:c.1974G>C
CA338451271
NM_001127660.2:c.1974G>T