Canonical Allele Identifier: PA2573259936
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1463011
ClinVar RCV Id: RCV001960843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asn311Ser
CA598962
NM_014874.4:c.932A>G