Canonical Allele Identifier: PA2829491707
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1744598
ClinVar RCV Id: RCV002342952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Thr1660Pro
CA412671858
NM_004009.3:c.4978A>C