Canonical Allele Identifier: PA2825766731
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6682
ClinVar RCV Id: RCV000007069 RCV000594920 RCV003159090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Gly331Trp
CA253918
NM_001130985.2:c.991G>T