Canonical Allele Identifier: PA2829493021
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 567722
ClinVar RCV Id: RCV000687887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Gln2509Pro
CA412658597
NM_004009.3:c.7526A>C