Canonical Allele Identifier: PA2829496342
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_004001.1:p.Thr879Ser
CA412667074
NM_004010.3:c.2636C>G
CA412667076
NM_004010.3:c.2635A>T