Canonical Allele Identifier: PA2829500017
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 567722
ClinVar RCV Id: RCV000687887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Gln1172Pro
CA412658597
NM_004011.4:c.3515A>C