Canonical Allele Identifier: PA204309
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2276
ClinVar RCV Id: RCV000002364 RCV000190245 RCV000200468 RCV000199279 RCV000415132 RCV001173686 RCV003162206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg94Trp
CA204307
NM_014874.4:c.280C>T