Canonical Allele Identifier: PA2829500662
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 520520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Ala1777Ser
CA10377828
NM_004011.4:c.5329G>T