Canonical Allele Identifier: PA1139721566
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 933228
ClinVar RCV Id: RCV001201342 RCV001876288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Lys307Glu
CA338441865
NM_014874.4:c.919A>G