Canonical Allele Identifier: PA2825649407
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637292
ClinVar RCV Id: RCV000789378 RCV001869222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Met376Arg
CA338443181
NM_001127660.2:c.1127T>G