Canonical Allele Identifier: PA2825649374
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 644078
ClinVar RCV Id: RCV000797918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Lys355del
CA915941134
NM_001127660.2:c.1064_1066del