Canonical Allele Identifier: PA2825649173
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637745
ClinVar RCV Id: RCV000790042 RCV003456430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Gly202Ala
CA338437692
NM_001127660.2:c.605G>C