Canonical Allele Identifier: PA2829494701
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 373618
ClinVar RCV Id: RCV000803894 RCV001697830 RCV002446637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Ser158Thr
CA10380042
NM_004010.3:c.473G>C