Canonical Allele Identifier: PA2825649800
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408322
ClinVar RCV Id: RCV000461042 RCV003133271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Leu741Val
CA16609871
NM_001127660.2:c.2221T>G