Canonical Allele Identifier: PA112549
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Arg523Gly
CA233294
NM_001005360.3:c.1567A>G