Canonical Allele Identifier: PA2829502572
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 598379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Trp1141Cys
CA10378272
NM_004012.4:c.3423G>T
CA412658894
NM_004012.4:c.3423G>C