Canonical Allele Identifier: PA658662798
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476770
ClinVar RCV Id: RCV000543497
ClinVar Variation Id: 1455514
ClinVar RCV Id: RCV001946636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg95Ser
CA338462188
NM_014874.4:c.285G>T
CA338462189
NM_014874.4:c.285G>C