Canonical Allele Identifier: PA2825767197
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471285
ClinVar RCV Id: RCV000550765 RCV001274454 RCV001558981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Arg798His
CA1706135
NM_001130985.2:c.2393G>A