Allele Registry

Canonical Allele Identifier: PA2825766498

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000647984

RCV001253301

ClinVar Variation:

538621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Asn103Ser	CA1705307 NM_001130985.2:c.308A>G