Canonical Allele Identifier: PA915997159
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447273
ClinVar RCV Id: RCV000516555 RCV000841305 RCV001088080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Asn734Ser
CA9201545
NM_001190716.1:c.2201A>G