Canonical Allele Identifier: PA2829489676
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 226566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ala569Val
CA10379745
NM_004009.3:c.1706C>T