Canonical Allele Identifier: PA2825649687
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501237
ClinVar RCV Id: RCV002017318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu644del
CA2580611409
NM_001127660.2:c.1930_1932del