Canonical Allele Identifier: PA2826162711
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 533827
ClinVar RCV Id: RCV000641096 RCV001507413 RCV002369681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Arg297Cys
CA9200925
NM_001190716.1:c.889C>T