Canonical Allele Identifier: PA2825649801
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476769
ClinVar RCV Id: RCV000530896 RCV001027507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu741Trp
CA338453887
NM_001127660.2:c.2222T>G