Canonical Allele Identifier: PA103054
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2278
ClinVar RCV Id: RCV000002367 RCV000023711 RCV000198024 RCV000195560 RCV000857103 RCV000857104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121132.1:p.Arg364Trp
CA115469
NM_001127660.2:c.1090C>T