Canonical Allele Identifier: PA2825757499
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288577
ClinVar RCV Id: RCV000647992 RCV000726189 RCV001271547
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Asn1613Ser
CA1707164
NM_001130980.2:c.4838A>G