Canonical Allele Identifier: PA112666
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7286
ClinVar RCV Id: RCV000007709 RCV003447079 RCV003441708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005360.1:p.Ser619Trp
CA254140
NM_001005360.3:c.1856C>G