Allele Registry

Canonical Allele Identifier: PA2829508059

Gene: DMD HGNC NCBI

ClinVar RCV:

RCV003151720

ClinVar Variation:

11236

HGVS (amino-acid)	Matching Registered Transcripts
NP_004010.1:p.Cys272Tyr	CA121414 NM_004019.3:c.815G>A