Canonical Allele Identifier: PA2825750066
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1491619
ClinVar RCV Id: RCV001988775 RCV003230723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Arg1025Gln
CA1706451
NM_001130977.2:c.3074G>A