Allele Registry

Canonical Allele Identifier: PA2826601019

Gene: DNM1L HGNC NCBI

ClinVar RCV:

RCV000239637

ClinVar Variation:

253261

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265395.1:p.Gly159Asp	CA10586275 NM_001278466.2:c.476G>A