Canonical Allele Identifier: PA2825649244
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392006
ClinVar RCV Id: RCV001882077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu246Asp
CA338439034
NM_001127660.2:c.738G>C
CA338439036
NM_001127660.2:c.738G>T