Canonical Allele Identifier: PA2825072090
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_000100.3:p.Thr994Ser
CA412667074
NM_000109.4:c.2981C>G
CA412667076
NM_000109.4:c.2980A>T