Canonical Allele Identifier: PA324237
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214634
ClinVar RCV Id: RCV000199695 RCV000692017 RCV001174302 RCV002399737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asn525Ser
CA324235
NM_014874.4:c.1574A>G