Canonical Allele Identifier: PA2825751789
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1409880
ClinVar RCV Id: RCV001939946 RCV003146344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Glu531Gly
CA49792919
NM_001130978.2:c.1592A>G