Canonical Allele Identifier: PA2829490118
Gene: DMD HGNC NCBI
ClinVar RCV:
RCV000012002
ClinVar Variation:
11251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Lys769Glu
CA341058
NM_004009.3:c.2305A>G