Canonical Allele Identifier: PA1139721686
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 957829
ClinVar RCV Id: RCV001230887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val354Gly
CA338442709
NM_014874.4:c.1061T>G