Canonical Allele Identifier: PA2825649098
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369728
ClinVar RCV Id: RCV000408641 RCV000789387 RCV001378252
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Asn131Ser
CA598814
NM_001127660.2:c.392A>G