Canonical Allele Identifier: PA323591
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214642
ClinVar RCV Id: RCV000199052 RCV000767173 RCV001087915 RCV001174298 RCV001099689 RCV001331980 RCV002444798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Cys281Ser
CA323589
NM_014874.4:c.842G>C
CA338441509
NM_014874.4:c.841T>A