Canonical Allele Identifier: PA2829501859
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1501149
ClinVar RCV Id: RCV002017248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Leu520Phe
CA412666502
NM_004012.4:c.1560G>T
CA412666505
NM_004012.4:c.1560G>C