Canonical Allele Identifier: PA323381
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala54Thr
CA323379
NM_014874.4:c.160G>A