Canonical Allele Identifier: PA2825071714
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11251
ClinVar RCV Id: RCV000012002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Lys765Glu
CA341058
NM_000109.4:c.2293A>G