Canonical Allele Identifier: PA1139719292
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 222546
ClinVar RCV Id: RCV000208075 RCV000213162 RCV001513398 RCV002354585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Gly1298Arg
CA076798
NM_004006.3:c.3892G>A
CA412670241
NM_004006.3:c.3892G>C