Canonical Allele Identifier: PA2829505323
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 520520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004005.2:p.Ala389Ser
CA10377828
NM_004014.3:c.1165G>T