Allele Registry

Canonical Allele Identifier: PA915974105

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000340111

RCV001086001

RCV001820813

RCV001835749

ClinVar Variation:

282423

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Ala1360Val	CA1706844 NM_001130982.2:c.4079C>T