Canonical Allele Identifier: PA658810037
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543232
ClinVar RCV Id: RCV000653938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.His361Pro
CA338442851
NM_014874.4:c.1082A>C