Canonical Allele Identifier: PA2825649010
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353075
ClinVar RCV Id: RCV001885439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu65Asp
CA338461620
NM_001127660.2:c.195A>C
CA338461622
NM_001127660.2:c.195A>T