Canonical Allele Identifier: PA645509565
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439898
ClinVar RCV Id: RCV000508148 RCV000559610 RCV001809462 RCV002431467
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Gln367His
CA599009
NM_014874.4:c.1101G>C
CA338442979
NM_014874.4:c.1101G>T