Allele Registry

Canonical Allele Identifier: PA172099

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000007704

RCV000145902

RCV000373773

RCV000641110

RCV001813964

ClinVar Variation:

7281

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005361.1:p.Arg465Trp	CA172098 NM_001005361.3:c.1393C>T