Canonical Allele Identifier: PA2499279432
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045262
ClinVar RCV Id: RCV001349644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asn683Ser
CA599306
NM_014874.4:c.2048A>G