Canonical Allele Identifier: PA2825649192
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30736
ClinVar RCV Id: RCV000023714 RCV000235670 RCV000456775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Phe216Ser
CA129420
NM_001127660.2:c.647T>C