Canonical Allele Identifier: PA2829494882
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 409929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Leu233Phe
CA10379978
NM_004010.3:c.697C>T