Canonical Allele Identifier: PA2826599129
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 253261
ClinVar RCV Id: RCV000239637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265392.1:p.Gly362Asp
CA10586275
NM_001278463.2:c.1085G>A