Canonical Allele Identifier: PA2829501606
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 264223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Thr339Ser
CA10378782
NM_004012.4:c.1016C>G
CA412671651
NM_004012.4:c.1015A>T