Canonical Allele Identifier: PA2829503251
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 520520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Ala1774Ser
CA10377828
NM_004012.4:c.5320G>T