Canonical Allele Identifier: PA2829509277
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 264219
ClinVar RCV Id: RCV000248044 RCV001067594 RCV001828166 RCV002479986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004012.2:p.Arg17Trp
CA10378279
NM_004021.3:c.49C>T