Canonical Allele Identifier: PA916001332
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 514651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Val972Leu
CA10379308
NM_004010.3:c.2914G>C