Canonical Allele Identifier: PA2825755392
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285686
ClinVar RCV Id: RCV000374736 RCV000664874 RCV000778917 RCV001563739 RCV001329706 RCV003940011
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Pro1770Gln
CA1707338
NM_001130979.2:c.5309C>A