Canonical Allele Identifier: PA1139721612
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 843133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala317Gly
CA338441986
NM_014874.4:c.950C>G