Canonical Allele Identifier: PA2829618696
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005681.2:p.Thr102Met
CA320842
NM_005690.5:c.305C>T