Canonical Allele Identifier: PA916028098
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 253262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317309.1:p.Gly375Ser
CA10586276
NM_001330380.2:c.1123G>A