Canonical Allele Identifier: PA1139719240
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 285018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Trp1265Ser
CA10379186
NM_004006.3:c.3794G>C