Canonical Allele Identifier: PA2573230335
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1501149
ClinVar RCV Id: RCV002017248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Leu523Phe
CA412666502
NM_004011.4:c.1569G>T
CA412666505
NM_004011.4:c.1569G>C