Canonical Allele Identifier: PA916028105
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 420713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317309.1:p.Cys444Tyr
CA16619510
NM_001330380.2:c.1331G>A