Canonical Allele Identifier: PA916001606
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Trp329Cys
CA295588
NM_004011.4:c.987G>T
CA412671780
NM_004011.4:c.987G>C