Canonical Allele Identifier: PA2829501657
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 423086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Leu373Phe
CA10378765
NM_004012.4:c.1117C>T