Canonical Allele Identifier: PA915969931
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637730
ClinVar RCV Id: RCV000790024 RCV001064640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu92Pro
CA338462142
NM_014874.4:c.275T>C