Canonical Allele Identifier: PA2825771112
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 969695
ClinVar RCV Id: RCV001245099 RCV001835223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Pro556Thr
CA1705879
NM_001130987.2:c.1666C>A