Canonical Allele Identifier: PA2829484567
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2052437
ClinVar RCV Id: RCV002932733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Val1688Ala
CA10378781
NM_004006.3:c.5063T>C