Canonical Allele Identifier: PA2825757819
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282408
ClinVar RCV Id: RCV000317613 RCV000754725 RCV002521880
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Tyr1894His
CA1707485
NM_001130980.2:c.5680T>C