Canonical Allele Identifier: PA115478
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2281
ClinVar RCV Id: RCV000002371 RCV000002370 RCV000144872 RCV000197230 RCV000515385 RCV000556047 RCV001267430 RCV003332995 RCV003332994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Arg104Trp
CA115475
NM_014874.4:c.310C>T