Canonical Allele Identifier: PA2826162776
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Arg369Trp
CA118658
NM_001190716.1:c.1105C>T