Canonical Allele Identifier: PA2825752299
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_001124450.1:p.Pro1019Leu
CA1706429
NM_001130978.2:c.3056C>T