Canonical Allele Identifier: PA2825072980
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1022986
ClinVar RCV Id: RCV001322971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Val1641Leu
CA412672060
NM_000109.4:c.4921G>T
CA412672062
NM_000109.4:c.4921G>C