Canonical Allele Identifier: PA2829493238
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 497501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Pro2691Ser
CA10378140
NM_004009.3:c.8071C>T