Canonical Allele Identifier: PA2829492062
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 374639
ClinVar RCV Id: RCV000416210 RCV003512038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Gln1863His
CA16043825
NM_004009.3:c.5589A>C
CA412666431
NM_004009.3:c.5589A>T