Canonical Allele Identifier: PA2825073337
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Ser1894Arg
CA10378618
NM_000109.4:c.5682C>A
CA412665704
NM_000109.4:c.5682C>G
CA412665715
NM_000109.4:c.5680A>C