Canonical Allele Identifier: PA2825649219
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543186
ClinVar RCV Id: RCV000653865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr232Pro
CA338438520
NM_001127660.2:c.694A>C