Canonical Allele Identifier: PA2825749659
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290745
ClinVar RCV Id: RCV000288710 RCV000311911 RCV000383412 RCV001139894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Gly666Val
CA1706038
NM_001130977.2:c.1997G>T