Canonical Allele Identifier: PA2825649429
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637310
ClinVar RCV Id: RCV000789410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Gln386Pro
CA338443417
NM_001127660.2:c.1157A>C
CA915941136
NM_001127660.2:c.1157_1158delinsCT