Canonical Allele Identifier: PA891847632
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578960
ClinVar RCV Id: RCV000702121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Gly606Ser
CA599229
NM_014874.4:c.1816G>A