Canonical Allele Identifier: PA172099
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7281
ClinVar RCV Id: RCV000007704 RCV000145902 RCV000373773 RCV000641110 RCV001813964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Arg465Trp
CA172098
NM_001005361.3:c.1393C>T