Canonical Allele Identifier: PA115471
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_055689.1:p.Arg364Trp
CA115469
NM_014874.4:c.1090C>T