Canonical Allele Identifier: PA2825649335
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1175732
ClinVar RCV Id: RCV001530990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu310Phe
CA338441902
NM_001127660.2:c.928C>T