Canonical Allele Identifier: PA2829484517
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Trp1670Cys
CA295588
NM_004006.3:c.5010G>T
CA412671780
NM_004006.3:c.5010G>C