Canonical Allele Identifier: PA2825071010
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 937961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Thr301Ser
CA412668467
NM_000109.4:c.902C>G
CA412668470
NM_000109.4:c.901A>T