Allele Registry

Canonical Allele Identifier: PA2829619057

Gene: DNM1L HGNC NCBI

ClinVar RCV:

RCV000239637

ClinVar Variation:

253261

HGVS (amino-acid)	Matching Registered Transcripts
NP_005681.2:p.Gly362Asp	CA10586275 NM_005690.5:c.1085G>A