Canonical Allele Identifier: PA915997029
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 158514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Arg522His
CA172101
NM_001190716.1:c.1565G>A