Canonical Allele Identifier: PA658810092
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543203
ClinVar RCV Id: RCV000653890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala738Thr
CA338453821
NM_014874.4:c.2212G>A