Canonical Allele Identifier: PA2825756859
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1442763
ClinVar RCV Id: RCV001953153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Tyr1051Cys
CA347217037
NM_001130980.2:c.3152A>G