Canonical Allele Identifier: PA2825649759
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402104
ClinVar RCV Id: RCV001913364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu711Asp
CA338453145
NM_001127660.2:c.2133G>C
CA338453147
NM_001127660.2:c.2133G>T