Allele Registry

Canonical Allele Identifier: PA357875

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000203274

ClinVar Variation:

218920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177645.1:p.Glu341Lys	CA339654 NM_001190716.1:c.1021G>A