Canonical Allele Identifier: PA2826162635
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423594
ClinVar RCV Id: RCV000481918 RCV001856877 RCV002367655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Pro226Leu
CA9200855
NM_001190716.1:c.677C>T