Canonical Allele Identifier: PA2825649389
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408317
ClinVar RCV Id: RCV000458626 RCV000991837 RCV001174304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr362Arg
CA16609879
NM_001127660.2:c.1085C>G