Canonical Allele Identifier: PA2825072457
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 196127
ClinVar Variation Id: 409920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Leu1264Phe
CA242962
NM_000109.4:c.3792G>C
CA16616498
NM_000109.4:c.3792G>T