Canonical Allele Identifier: PA2825748859
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 287816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Arg1986Gln
CA1707599
NM_001130976.2:c.5957G>A