Canonical Allele Identifier: PA1139721300
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 835548
ClinVar RCV Id: RCV001036451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asp210Gly
CA338437864
NM_014874.4:c.629A>G