Canonical Allele Identifier: PA2829496705
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 196127
ClinVar Variation Id: 409920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Leu1149Phe
CA242962
NM_004010.3:c.3447G>C
CA16616498
NM_004010.3:c.3447G>T