Canonical Allele Identifier: PA2826601018
Gene: DNM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 253262
ClinVar RCV Id: RCV000239681 RCV001557633 RCV003897583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265395.1:p.Gly159Ser
CA10586276
NM_001278466.2:c.475G>A