Canonical Allele Identifier: PA2825649511
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2282
ClinVar RCV Id: RCV000002372 RCV000196650 RCV000312138 RCV000487518 RCV001086652 RCV001172693 RCV001814957 RCV002390086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg468His
CA252169
NM_001127660.2:c.1403G>A