Canonical Allele Identifier: PA115468
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2277
ClinVar RCV Id: RCV000002366 RCV001253214 RCV002426481 RCV003482223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Gln276Arg
CA115466
NM_014874.4:c.827A>G