Canonical Allele Identifier: PA2825649344
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala317Ser
CA338441982
NM_001127660.2:c.949G>T