Canonical Allele Identifier: PA2825649137
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.His165Asp
CA252163
NM_001127660.2:c.493C>G