Canonical Allele Identifier: PA2829492900
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Arg2411Cys
CA233490
NM_004009.3:c.7231C>T