Canonical Allele Identifier: PA2825073060
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2173940
ClinVar RCV Id: RCV002584851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Lys1701Asn
CA412671467
NM_000109.4:c.5103A>C
CA412671468
NM_000109.4:c.5103A>T