Canonical Allele Identifier: PA2829497585
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Ser1779Arg
CA10378618
NM_004010.3:c.5337C>A
CA412665704
NM_004010.3:c.5337C>G
CA412665715
NM_004010.3:c.5335A>C