Canonical Allele Identifier: PA2829491719
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1061899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Glu1665Asp
CA10378809
NM_004009.3:c.4995G>C
CA412671794
NM_004009.3:c.4995G>T