Canonical Allele Identifier: PA658810060
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 523025
ClinVar RCV Id: RCV000626228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg476Gly
CA338446686
NM_014874.4:c.1426C>G