Canonical Allele Identifier: PA2825649270
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637279
ClinVar RCV Id: RCV000789362 RCV000796767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg259Leu
CA338439249
NM_001127660.2:c.776G>T