Canonical Allele Identifier: PA2829489680
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 94478
ClinVar RCV Id: RCV000235164 RCV000619753 RCV000723549 RCV001079116 RCV001831832 RCV004542773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Glu573Asp
CA285532
NM_004009.3:c.1719A>T
CA412673244
NM_004009.3:c.1719A>C