Allele Registry

Canonical Allele Identifier: PA172097

Gene: DNM2 HGNC NCBI

ClinVar RCV:

RCV000145901

ClinVar Variation:

158513

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005361.1:p.Val375Glu	CA172095 NM_001005361.3:c.1124T>A