Canonical Allele Identifier: PA645477627
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283977
ClinVar RCV Id: RCV000271598 RCV000356959 RCV000366269 RCV000695150 RCV001271793 RCV002487214
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Arg826Gln
CA1706183
NM_001130987.2:c.2477G>A