Canonical Allele Identifier: PA2825768924
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538634
ClinVar RCV Id: RCV000648001 RCV001004972 RCV001563954 RCV001563955 RCV001756080
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Asn264Ser
CA1705487
NM_001130986.2:c.791A>G