Canonical Allele Identifier: PA658810026
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543222
ClinVar RCV Id: RCV000653918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala306Thr
CA338441851
NM_014874.4:c.916G>A