Canonical Allele Identifier: PA2829492397
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1751843
ClinVar RCV Id: RCV002360391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ser2044Ile
CA412666501
NM_004009.3:c.6131G>T