Canonical Allele Identifier: PA645477618
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 195749
ClinVar RCV Id: RCV000176395 RCV000765697 RCV001085145 RCV001271790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly779Ser
CA242326
NM_001130987.2:c.2335G>A