Canonical Allele Identifier: PA645407344
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Asn131Ser
CA598814
NM_014874.4:c.392A>G