Canonical Allele Identifier: PA658809981
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543168
ClinVar RCV Id: RCV000653837 RCV001566325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ile88Met
CA338462084
NM_014874.4:c.264C>G