Allele Registry

Canonical Allele Identifier: PA2829469100

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000596899

ClinVar Variation:

501582

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Cys1971Arg	CA347226529 NM_003494.4:c.5911T>C