Canonical Allele Identifier: PA2825649420
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543189
ClinVar RCV Id: RCV000653868 RCV000789364 RCV003482291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala382Pro
CA338443308
NM_001127660.2:c.1144G>C