Canonical Allele Identifier: PA645407454
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu744Lys
CA16616967
NM_014874.4:c.2230G>A