Canonical Allele Identifier: PA118657
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7279
ClinVar RCV Id: RCV000007702 RCV000145900 RCV000701394 RCV001781202
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Arg369Gln
CA118655
NM_001005362.3:c.1106G>A