Canonical Allele Identifier: PA2825746770
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284469
ClinVar RCV Id: RCV000596973 RCV000725459 RCV003736685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Val69Gly
CA10604804
NM_001130976.2:c.206T>G