Canonical Allele Identifier: PA658662800
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Lys98Glu
CA338462271
NM_014874.4:c.292A>G