Canonical Allele Identifier: PA2825071086
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 409929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Leu348Phe
CA10379978
NM_000109.4:c.1042C>T