Canonical Allele Identifier: PA2829492057
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_004000.1:p.Leu1860Phe
CA412666502
NM_004009.3:c.5580G>T
CA412666505
NM_004009.3:c.5580G>C