Canonical Allele Identifier: PA2829490690
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 368249
ClinVar RCV Id: RCV000370724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ile1053Val
CA10653907
NM_004009.3:c.3157A>G