Allele Registry

Canonical Allele Identifier: PA2829467248

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 336964

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Thr1036Ile	CA1706444 NM_003494.4:c.3107C>T