Canonical Allele Identifier: PA2829506822
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1448670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004008.1:p.Thr21Ser
CA10377852
NM_004017.3:c.61A>T