Canonical Allele Identifier: PA292080
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138217
ClinVar RCV Id: RCV000126754 RCV000227305 RCV000711273 RCV001101762 RCV001173010 RCV002492476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val705Ile
CA292078
NM_014874.4:c.2113G>A