Canonical Allele Identifier: PA2825759494
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289963
ClinVar RCV Id: RCV001086957 RCV000726406 RCV001271534 RCV003910035
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Asn1368Ser
CA1706892
NM_001130981.2:c.4103A>G