Canonical Allele Identifier: PA2825649135
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217164
ClinVar RCV Id: RCV000201063 RCV000235729 RCV000653851 RCV003338460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.His165Arg
CA279075
NM_001127660.2:c.494A>G