Canonical Allele Identifier: PA2741948051
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883385
ClinVar RCV Id: RCV003743407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ile368Val
CA338442989
NM_014874.4:c.1102A>G