Canonical Allele Identifier: PA2829492071
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1036102
ClinVar RCV Id: RCV001339055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Lys1867Met
CA412666340
NM_004009.3:c.5600A>T