Canonical Allele Identifier: PA915970099
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 801443
ClinVar RCV Id: RCV000986244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ile213Asn
CA338437954
NM_014874.4:c.638T>A