Canonical Allele Identifier: PA279066
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217163
ClinVar RCV Id: RCV000201006 RCV000237022 RCV001386993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu146Phe
CA279064
NM_014874.4:c.436C>T