Canonical Allele Identifier: PA2825747370
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283484
ClinVar RCV Id: RCV000348203 RCV001466761 RCV001823130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gly639Ser
CA1706026
NM_001130976.2:c.1915G>A