Allele Registry

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Canonical Allele Identifier: PA915970131

Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637299

ClinVar RCV Id: RCV000789389 RCV003581716

ClinVar Variation Id: 836052

ClinVar RCV Id: RCV001037085 RCV001331979

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Phe223Leu	CA338438267 NM_014874.4:c.667T>C CA338438282 NM_014874.4:c.669T>A CA338438287 NM_014874.4:c.669T>G