Canonical Allele Identifier: PA645407309
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr60Met
CA598770
NM_014874.4:c.179C>T