Canonical Allele Identifier: PA645407367
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 243066
ClinVar RCV Id: RCV000235053 RCV000693266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val244Met
CA10584074
NM_014874.4:c.730G>A