Canonical Allele Identifier: PA2829502132
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 662549
ClinVar RCV Id: RCV000820213 RCV001825654 RCV003145205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Ser721Ile
CA10378515
NM_004012.4:c.2162G>T