Canonical Allele Identifier: PA2825071852
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 388597
ClinVar RCV Id: RCV000432155 RCV000630562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Thr850Ser
CA10379493
NM_000109.4:c.2548A>T
CA412671988
NM_000109.4:c.2549C>G