Canonical Allele Identifier: PA2829508135
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2161204
ClinVar RCV Id: RCV003078453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004011.3:p.Leu7Ser
CA412659010
NM_004020.4:c.20T>C