Canonical Allele Identifier: PA2825766092
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282624
ClinVar RCV Id: RCV000266653 RCV000725114 RCV000757894 RCV001141002 RCV001810440 RCV003463743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Arg1776Gln
CA1707357
NM_001130984.2:c.5327G>A