Canonical Allele Identifier: PA2825649774
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444862
ClinVar RCV Id: RCV001956012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Glu722Asp
CA599350
NM_001127660.2:c.2166G>C
CA338453277
NM_001127660.2:c.2166G>T