Canonical Allele Identifier: PA2829490118
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 11251
ClinVar RCV Id: RCV000012002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Lys769Glu
CA341058
NM_004009.3:c.2305A>G