Allele Registry

Canonical Allele Identifier: PA915997111

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000255790

ClinVar Variation:

265656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177645.1:p.Pro627Ala	CA10588681 NM_001190716.1:c.1879C>G