Canonical Allele Identifier: PA2829491631
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 409879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ile1617Thr
CA10378834
NM_004009.3:c.4850T>C