Canonical Allele Identifier: PA2825649796
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408331
ClinVar RCV Id: RCV000458069
ClinVar Variation Id: 637723
ClinVar RCV Id: RCV000790016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Trp740Cys
CA16609875
NM_001127660.2:c.2220G>T
CA338453880
NM_001127660.2:c.2220G>C