Allele Registry

Canonical Allele Identifier: PA2829501657

Gene: DMD HGNC NCBI

ClinVar RCV:

RCV000485408

RCV003512049

ClinVar Variation:

423086

HGVS (amino-acid)	Matching Registered Transcripts
NP_004003.2:p.Leu373Phe	CA10378765 NM_004012.4:c.1117C>T