Canonical Allele Identifier: PA915970330
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637286
ClinVar RCV Id: RCV000789371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu329del
CA915941132
NM_014874.4:c.986_988del