Canonical Allele Identifier: PA916001158
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 498390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Arg26Ser
CA10380156
NM_004010.3:c.76C>A