Canonical Allele Identifier: PA915997162
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 465284
ClinVar RCV Id: RCV000547445 RCV000834573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177645.1:p.Val744Ala
CA9201548
NM_001190716.1:c.2231T>C