Canonical Allele Identifier: PA270655
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 155730
ClinVar RCV Id: RCV000143799 RCV000197364 RCV000653884 RCV000789066 RCV002408639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg259Cys
CA270652
NM_014874.4:c.775C>T