Canonical Allele Identifier: PA2829468274
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538640
ClinVar RCV Id: RCV000648011 RCV001563808 RCV001563809 RCV001563807
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Ile1584Val
CA1707160
NM_003494.4:c.4750A>G