Canonical Allele Identifier: PA2829509339
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 501821
ClinVar RCV Id: RCV000591545 RCV000694041 RCV001834905 RCV002395538 RCV002498865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004012.2:p.Glu69Gln
CA10378248
NM_004021.3:c.205G>C