Canonical Allele Identifier: PA2825761939
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 834151
ClinVar RCV Id: RCV001034779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Ala2104Val
CA1707696
NM_001130982.2:c.6311C>T