Canonical Allele Identifier: PA2825694224
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 652065
ClinVar RCV Id: RCV000807552 RCV001825604
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Pro1020Leu
CA1706429
NM_001130455.2:c.3059C>T