Canonical Allele Identifier: PA2829488849
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11279
ClinVar RCV Id: RCV000012030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Thr275Ala
CA255770
NM_004009.3:c.823A>G