Canonical Allele Identifier: PA2829502469
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290200
ClinVar RCV Id: RCV001078740 RCV003165774 RCV001828275 RCV000261998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Pro1033Leu
CA10378333
NM_004012.4:c.3098C>T