Canonical Allele Identifier: PA2829495669
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 498354
ClinVar RCV Id: RCV000591854 RCV000696509 RCV001829644 RCV002431747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Phe627Ser
CA10379593
NM_004010.3:c.1880T>C