Canonical Allele Identifier: PA2825649264
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2122398
ClinVar RCV Id: RCV003054027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ile255Thr
CA338439185
NM_001127660.2:c.764T>C