Canonical Allele Identifier: PA2829491709
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2047955
ClinVar RCV Id: RCV002918433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ser1661Cys
CA412671839
NM_004009.3:c.4982C>G