Canonical Allele Identifier: PA2825649280
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246495
ClinVar RCV Id: RCV000236640 RCV000818378 RCV001027467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Met270Thr
CA598921
NM_001127660.2:c.809T>C