Canonical Allele Identifier: PA112628
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7277
ClinVar RCV Id: RCV000007700 RCV000789618 RCV003447076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Lys562Glu
CA118652
NM_001005360.3:c.1684A>G