Canonical Allele Identifier: PA2825649057
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 546588
ClinVar RCV Id: RCV000658492 RCV000790051 RCV000707644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala100Gly
CA338462338
NM_001127660.2:c.299C>G