Canonical Allele Identifier: PA2825073012
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1369894
ClinVar RCV Id: RCV001899192 RCV002482568 RCV002343931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Leu1666Phe
CA222419
NM_000109.4:c.4998G>C
CA412671749
NM_000109.4:c.4998G>T