Canonical Allele Identifier: PA2829506788
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 263511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004007.1:p.Ser579Asn
CA10377501
NM_004016.3:c.1736G>A