Allele Registry

Canonical Allele Identifier: PA2829491049

Gene: DMD HGNC NCBI

ClinVar RCV:

RCV000394586

RCV000547718

RCV001169829

RCV001795483

RCV001835753

ClinVar Variation:

285018

HGVS (amino-acid)	Matching Registered Transcripts
NP_004000.1:p.Trp1261Ser	CA10379186 NM_004009.3:c.3782G>C