Canonical Allele Identifier: PA2825649064
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214652
ClinVar RCV Id: RCV000201133 RCV000462918 RCV001090177 RCV001726042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr105Met
CA279096
NM_001127660.2:c.314C>T