Canonical Allele Identifier: PA645477818
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284471
ClinVar RCV Id: RCV000265900 RCV001859602 RCV003401247
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val1879Met
CA10604806
NM_001130987.2:c.5635G>A