Canonical Allele Identifier: PA2825649757
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575589
ClinVar RCV Id: RCV000697850 RCV000789408 RCV002468601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu710Pro
CA338453131
NM_001127660.2:c.2129T>C