Canonical Allele Identifier: PA2573091029
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala660Thr
CA599290
NM_014874.4:c.1978G>A