Canonical Allele Identifier: PA2825649707
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442524
ClinVar RCV Id: RCV001953043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala660Asp
CA599291
NM_001127660.2:c.1979C>A