Canonical Allele Identifier: PA2829496008
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 388597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Thr735Ser
CA10379493
NM_004010.3:c.2203A>T
CA412671988
NM_004010.3:c.2204C>G