Canonical Allele Identifier: PA2825749221
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 198494
ClinVar RCV Id: RCV000656845 RCV000706741 RCV001276722 RCV001336579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Asn236Thr
CA247174
NM_001130977.2:c.707A>C