Canonical Allele Identifier: PA915970553
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 694953
ClinVar RCV Id: RCV000857111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asn683His
CA338451690
NM_014874.4:c.2047A>C