Allele Registry

Canonical Allele Identifier: PA2826162782

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV001902272

ClinVar Variation:

1363462

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177645.1:p.Val375Ala	CA404048089 NM_001190716.1:c.1124T>C