Canonical Allele Identifier: PA2829497254
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Trp1547Cys
CA295588
NM_004010.3:c.4641G>T
CA412671780
NM_004010.3:c.4641G>C