Canonical Allele Identifier: PA2825649138
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439897
ClinVar RCV Id: RCV000506106 RCV000789411 RCV000802072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.His165Tyr
CA338436254
NM_001127660.2:c.493C>T