Canonical Allele Identifier: PA2573260058
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1358907
ClinVar RCV Id: RCV001864195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu673Met
CA338451566
NM_014874.4:c.2017C>A