Canonical Allele Identifier: PA2825649233
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220333
ClinVar RCV Id: RCV000205521
ClinVar Variation Id: 437424
ClinVar RCV Id: RCV000502695
ClinVar Variation Id: 694947
ClinVar RCV Id: RCV000857098 RCV001858529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Phe240Leu
CA349675
NM_001127660.2:c.720C>A
CA338438888
NM_001127660.2:c.718T>C
CA338438901
NM_001127660.2:c.720C>G