Canonical Allele Identifier: PA2829501919
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290556
ClinVar RCV Id: RCV000329015 RCV001231485 RCV001833409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Ser558Arg
CA10378618
NM_004012.4:c.1674C>A
CA412665704
NM_004012.4:c.1674C>G
CA412665715
NM_004012.4:c.1672A>C