Canonical Allele Identifier: PA2825753668
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94334
ClinVar RCV Id: RCV000080300 RCV000531528 RCV001273964 RCV001699034 RCV001449921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Ala201Glu
CA147766
NM_001130979.2:c.602C>A