Canonical Allele Identifier: PA2829502837
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 264464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Trp1394Arg
CA10378131
NM_004012.4:c.4180T>C
CA412657055
NM_004012.4:c.4180T>A