Allele Registry

Canonical Allele Identifier: PA916001141

Gene: DMD HGNC NCBI

ClinVar RCV:

RCV000614194

RCV001050261

RCV001256878

RCV002438577

ClinVar Variation:

511426

HGVS (amino-acid)	Matching Registered Transcripts
NP_004000.1:p.Thr998Ser	CA412667074 NM_004009.3:c.2993C>G CA412667076 NM_004009.3:c.2992A>T