Canonical Allele Identifier: PA2829511119
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1448670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004013.2:p.Thr629Ser
CA10377852
NM_004022.3:c.1885A>T