Canonical Allele Identifier: PA2826599152
Gene: DNM1L HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265392.1:p.Glu379Lys
CA16043679
NM_001278463.2:c.1135G>A