Canonical Allele Identifier: PA319827
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg300Cys
CA319825
NM_014874.4:c.898C>T