Canonical Allele Identifier: PA2825649189
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575481
ClinVar RCV Id: RCV000697709 RCV000789396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ile213Thr
CA338437956
NM_001127660.2:c.638T>C