Canonical Allele Identifier: PA915970306
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637301
ClinVar RCV Id: RCV000789391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Phe284Tyr
CA338441572
NM_014874.4:c.851T>A