Canonical Allele Identifier: PA915970544
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu673Pro
CA338451573
NM_014874.4:c.2018T>C