Canonical Allele Identifier: PA103128
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2274
ClinVar RCV Id: RCV000002362 RCV000547064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Lys357Asn
CA252160
NM_001127660.2:c.1071G>C
CA338442770
NM_001127660.2:c.1071G>T