Canonical Allele Identifier: PA2829491696
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1393817
ClinVar RCV Id: RCV001884632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ser1650Gly
CA412671991
NM_004009.3:c.4948A>G