Canonical Allele Identifier: PA2825766901
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 194354
ClinVar RCV Id: RCV000174707 RCV000674572 RCV003468855
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Leu480Pro
CA240279
NM_001130985.2:c.1439T>C