Allele Registry

Canonical Allele Identifier: PA2825758125

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000647984

RCV001253301

ClinVar Variation:

538621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Asn102Ser	CA1705307 NM_001130981.2:c.305A>G