Canonical Allele Identifier: PA2829486392
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2826985
ClinVar RCV Id: RCV003622850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Arg2497Ser
CA412658802
NM_004006.3:c.7491G>T
CA412658804
NM_004006.3:c.7491G>C