Canonical Allele Identifier: PA645476979
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289471
ClinVar RCV Id: RCV000536797 RCV000711545 RCV001835762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val43Met
CA1705230
NM_001130987.2:c.127G>A