Canonical Allele Identifier: PA2825649005
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246508
ClinVar RCV Id: RCV000236416 RCV000275642 RCV000653930 RCV002411073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Thr60Met
CA598770
NM_001127660.2:c.179C>T