Canonical Allele Identifier: PA2829499961
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2161204
ClinVar RCV Id: RCV003078453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Leu1126Ser
CA412659010
NM_004011.4:c.3377T>C