Canonical Allele Identifier: PA916002098
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 449172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Arg850Gln
CA10378442
NM_004011.4:c.2549G>A