Canonical Allele Identifier: PA645477546
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6682
ClinVar RCV Id: RCV000007069 RCV000594920 RCV003159090
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly331Trp
CA253918
NM_001130987.2:c.991G>T