Canonical Allele Identifier: PA2825649764
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466964
ClinVar RCV Id: RCV001970284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Ala716Ser
CA599343
NM_001127660.2:c.2146G>T