Canonical Allele Identifier: PA2825649068
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476771
ClinVar RCV Id: RCV000544862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ser106Arg
CA338433816
NM_001127660.2:c.316A>C
CA338433852
NM_001127660.2:c.318C>A
CA338433854
NM_001127660.2:c.318C>G