Allele Registry

Canonical Allele Identifier: PA118669

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000007707

RCV000789619

RCV003447078

ClinVar Variation:

7284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005361.1:p.Leu570His	CA118667 NM_001005361.3:c.1709T>A