Canonical Allele Identifier: PA2829504057
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 409922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004004.2:p.Ala287Thr
CA10378103
NM_004013.3:c.859G>A