Canonical Allele Identifier: PA2825755185
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285741
ClinVar RCV Id: RCV000306735 RCV000338437 RCV001055238 RCV000406757 RCV001833354 RCV002519192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Pro1586Ser
CA1707143
NM_001130979.2:c.4756C>T