Canonical Allele Identifier: PA2825750683
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538640
ClinVar RCV Id: RCV000648011 RCV001563808 RCV001563809 RCV001563807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Ile1591Val
CA1707160
NM_001130977.2:c.4771A>G