Canonical Allele Identifier: PA2825071416
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 94478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Glu569Asp
CA285532
NM_000109.4:c.1707A>T
CA412673244
NM_000109.4:c.1707A>C