Canonical Allele Identifier: PA2825649040
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 581439
ClinVar RCV Id: RCV000705260 RCV000857089 RCV001353161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Val91Leu
CA338462122
NM_001127660.2:c.271G>C
CA338462123
NM_001127660.2:c.271G>T