Canonical Allele Identifier: PA2829491724
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Trp1666Cys
CA295588
NM_004009.3:c.4998G>T
CA412671780
NM_004009.3:c.4998G>C