Canonical Allele Identifier: PA2825649773
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 569239
ClinVar RCV Id: RCV000689817 RCV002424610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ile721Thr
CA599349
NM_001127660.2:c.2162T>C