Canonical Allele Identifier: PA2825648969
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214656
ClinVar RCV Id: RCV000342413 RCV000556563 RCV000789062 RCV001705126 RCV002354554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.His20Tyr
CA321399
NM_001127660.2:c.58C>T