Canonical Allele Identifier: PA103119
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2270
ClinVar RCV Id: RCV000002358 RCV000200837 RCV000653847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu76Pro
CA252148
NM_001127660.2:c.227T>C