Canonical Allele Identifier: PA103138
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Pro251Ala
CA252154
NM_001127660.2:c.751C>G