Canonical Allele Identifier: PA2829501585
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 166757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Trp326Cys
CA295588
NM_004012.4:c.978G>T
CA412671780
NM_004012.4:c.978G>C