Canonical Allele Identifier: PA2825649528
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2084071
ClinVar RCV Id: RCV002994519 RCV003269382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ser483Phe
CA338446791
NM_001127660.2:c.1448C>T