Canonical Allele Identifier: PA2829491049
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 285018
ClinVar RCV Id: RCV000394586 RCV000547718 RCV001169829 RCV001795483 RCV001835753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Trp1261Ser
CA10379186
NM_004009.3:c.3782G>C