Canonical Allele Identifier: PA2829483443
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 511426
ClinVar RCV Id: RCV000614194 RCV001050261 RCV001256878 RCV002438577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003997.2:p.Thr1002Ser
CA412667074
NM_004006.3:c.3005C>G
CA412667076
NM_004006.3:c.3004A>T