Canonical Allele Identifier: PA279089
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217161
ClinVar RCV Id: RCV000793093 RCV001542541 RCV001552650 RCV002051828 RCV002444815 RCV004530201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Met376Val
CA279087
NM_014874.4:c.1126A>G