Canonical Allele Identifier: PA2825649055
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447723
ClinVar RCV Id: RCV000518242 RCV000790050 RCV001360038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Lys98Glu
CA338462271
NM_001127660.2:c.292A>G