Canonical Allele Identifier: PA129425
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30738
ClinVar RCV Id: RCV000023716 RCV000240513 RCV000857102 RCV001198485 RCV001388766 RCV002472935 RCV002415428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr362Met
CA129423
NM_014874.4:c.1085C>T