Canonical Allele Identifier: PA2825073002
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1061899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Glu1661Asp
CA10378809
NM_000109.4:c.4983G>C
CA412671794
NM_000109.4:c.4983G>T