Canonical Allele Identifier: PA118653
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Lys558Glu
CA118652
NM_001005362.3:c.1672A>G