Canonical Allele Identifier: PA2829507054
Gene: DMD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004008.1:p.Cys272Tyr
CA121414
NM_004017.3:c.815G>A