Canonical Allele Identifier: PA658810010
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543186
ClinVar RCV Id: RCV000653865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr232Pro
CA338438520
NM_014874.4:c.694A>C