Canonical Allele Identifier: PA2573260068
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402104
ClinVar RCV Id: RCV001913364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu711Asp
CA338453145
NM_014874.4:c.2133G>C
CA338453147
NM_014874.4:c.2133G>T