Canonical Allele Identifier: PA2829492995
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2826985
ClinVar RCV Id: RCV003622850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Arg2493Ser
CA412658802
NM_004009.3:c.7479G>T
CA412658804
NM_004009.3:c.7479G>C