Canonical Allele Identifier: PA2825074001
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2826985
ClinVar RCV Id: RCV003622850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Arg2489Ser
CA412658802
NM_000109.4:c.7467G>T
CA412658804
NM_000109.4:c.7467G>C