Canonical Allele Identifier: PA2829485297
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Ser1902Arg
CA10378618
NM_004006.3:c.5706C>A
CA412665704
NM_004006.3:c.5706C>G
CA412665715
NM_004006.3:c.5704A>C