Canonical Allele Identifier: PA2499279429
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006464
ClinVar RCV Id: RCV001303510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Phe661Leu
CA338451294
NM_014874.4:c.1981T>C
CA338451308
NM_014874.4:c.1983C>G
CA338451310
NM_014874.4:c.1983C>A