Canonical Allele Identifier: PA1139722156
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 917375
ClinVar RCV Id: RCV001174315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg707_Asn709del
CA1139655976
NM_014874.4:c.2120_2128del