Allele Registry

Canonical Allele Identifier: PA2826162774

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000236677

ClinVar Variation:

245905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177645.1:p.Arg369Leu	CA10584604 NM_001190716.1:c.1106G>T