Canonical Allele Identifier: PA2829503770
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 264219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004004.2:p.Arg17Trp
CA10378279
NM_004013.3:c.49C>T