Canonical Allele Identifier: PA2580378260
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006256
ClinVar RCV Id: RCV002811660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Glu271Asp
CA338439545
NM_014874.4:c.813G>C
CA338439550
NM_014874.4:c.813G>T