Canonical Allele Identifier: PA321155
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214649
ClinVar RCV Id: RCV000334497 RCV000554698 RCV000731890 RCV000790008 RCV002426935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala716Thr
CA321153
NM_014874.4:c.2146G>A