Canonical Allele Identifier: PA2825073000
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1395206
ClinVar RCV Id: RCV001891327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Ala1659Val
CA10378810
NM_000109.4:c.4976C>T