Canonical Allele Identifier: PA2825649254
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214653
ClinVar RCV Id: RCV000464315 RCV000789405 RCV000767172 RCV001706178 RCV002390522 RCV004530168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg250Gln
CA325008
NM_001127660.2:c.749G>A