Canonical Allele Identifier: PA2825756788
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282765
ClinVar RCV Id: RCV000270967 RCV000325795 RCV000725139 RCV001084284 RCV001272823 RCV003920053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Lys1000Thr
CA1706371
NM_001130980.2:c.2999A>C