Canonical Allele Identifier: PA645407347
Gene: MFN2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val160Gly
CA10584072
NM_014874.4:c.479T>G