Canonical Allele Identifier: PA915970599
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637062
ClinVar RCV Id: RCV000789069 RCV003581709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu734Val
CA338453441
NM_014874.4:c.2200C>G