Canonical Allele Identifier: PA118669
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7284
ClinVar RCV Id: RCV000007707 RCV000789619 RCV003447078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Leu570His
CA118667
NM_001005361.3:c.1709T>A