Canonical Allele Identifier: PA118666
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7283
ClinVar RCV Id: RCV000007706 RCV000789617 RCV003447077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005361.1:p.Gly537Cys
CA118664
NM_001005361.3:c.1609G>T