Canonical Allele Identifier: PA110877
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6678
ClinVar RCV Id: RCV000007065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Glu1734Gly
CA253911
NM_003494.4:c.5201A>G