Canonical Allele Identifier: PA2825749631
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283484
ClinVar RCV Id: RCV000348203 RCV001466761 RCV001823130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Gly639Ser
CA1706026
NM_001130977.2:c.1915G>A