Canonical Allele Identifier: PA2829506014
Gene: DMD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004006.1:p.Arg302Pro
CA412652922
NM_004015.3:c.905G>C