Canonical Allele Identifier: PA2825649397
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439898
ClinVar RCV Id: RCV000508148 RCV000559610 RCV001809462 RCV002431467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Gln367His
CA599009
NM_001127660.2:c.1101G>C
CA338442979
NM_001127660.2:c.1101G>T