Canonical Allele Identifier: PA2829509296
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2826985
ClinVar RCV Id: RCV003622850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004012.2:p.Arg37Ser
CA412658802
NM_004021.3:c.111G>T
CA412658804
NM_004021.3:c.111G>C