Canonical Allele Identifier: PA103042
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2271
ClinVar RCV Id: RCV000002359 RCV000236600 RCV000549934 RCV000789418 RCV001836692 RCV002468552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg280His
CA252151
NM_001127660.2:c.839G>A