Canonical Allele Identifier: PA658662852
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449524
ClinVar RCV Id: RCV000519202 RCV000789395 RCV000689677 RCV003483651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val273Gly
CA338441387
NM_014874.4:c.818T>G