Canonical Allele Identifier: PA2573259911
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1526418
ClinVar RCV Id: RCV002052434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val222Leu
CA338438236
NM_014874.4:c.664G>T
CA338438242
NM_014874.4:c.664G>C