Canonical Allele Identifier: PA2825073022
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 264223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Thr1675Ser
CA10378782
NM_000109.4:c.5024C>G
CA412671651
NM_000109.4:c.5023A>T