Canonical Allele Identifier: PA2825769941
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452908
ClinVar RCV Id: RCV000765698 RCV000727399 RCV001485096 RCV001563734 RCV001563735 RCV001272834
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Pro1201Leu
CA1706667
NM_001130986.2:c.3602C>T