Canonical Allele Identifier: PA645407350
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 243074
ClinVar RCV Id: RCV000235058 RCV001007825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Gly176Ser
CA10584073
NM_014874.4:c.526G>A