Canonical Allele Identifier: PA2826162705
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 647676
ClinVar RCV Id: RCV000802235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Arg290Gly
CA404046178
NM_001190716.1:c.868C>G