Canonical Allele Identifier: PA252159
Gene: MFN2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val69Phe
CA252157
NM_014874.4:c.205G>T