Canonical Allele Identifier: PA916028089
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317309.1:p.Thr115Met
CA320842
NM_001330380.2:c.344C>T