Canonical Allele Identifier: PA916028101
Gene: DNM1L HGNC NCBI
ClinVar RCV:
RCV000414839
ClinVar Variation:
374321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317309.1:p.Glu392Lys
CA16043679
NM_001330380.2:c.1174G>A