Canonical Allele Identifier: PA2825072965
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1064318
ClinVar RCV Id: RCV001374271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Leu1634Phe
CA412672151
NM_000109.4:c.4902G>T
CA412672153
NM_000109.4:c.4902G>C