Canonical Allele Identifier: PA2829496607
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1505008
ClinVar RCV Id: RCV002020272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Asp1068Gly
CA10379244
NM_004010.3:c.3203A>G