Canonical Allele Identifier: PA2829511628
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2897622
ClinVar RCV Id: RCV003623905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004014.2:p.Ala13Val
CA412658971
NM_004023.3:c.38C>T