Canonical Allele Identifier: PA2573260070
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_055689.1:p.Ala716Ser
CA599343
NM_014874.4:c.2146G>T