Canonical Allele Identifier: PA2825767502
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 661790
ClinVar RCV Id: RCV000819285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.His1055Tyr
CA1706445
NM_001130985.2:c.3163C>T