Canonical Allele Identifier: PA103160
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2269
ClinVar RCV Id: RCV000002357 RCV000197403 RCV000235811 RCV000763240 RCV000857112 RCV001001747 RCV002426480 RCV002444413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Trp740Ser
CA252145
NM_001127660.2:c.2219G>C