Canonical Allele Identifier: PA2825649027
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 949776
ClinVar RCV Id: RCV001221318 RCV002269347 RCV002429939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ser83Cys
CA18038726
NM_001127660.2:c.248C>G