Canonical Allele Identifier: PA645407356
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Leu218Pro
CA10584097
NM_014874.4:c.653T>C