Canonical Allele Identifier: PA118665
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Gly533Cys
CA118664
NM_001005362.3:c.1597G>T