Canonical Allele Identifier: PA118656
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7279
ClinVar RCV Id: RCV000007702 RCV000145900 RCV000701394 RCV001781202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Arg369Gln
CA118655
NM_001005361.3:c.1106G>A