Canonical Allele Identifier: PA2825751797
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538642
ClinVar RCV Id: RCV000648014 RCV001829805 RCV003243237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Glu541Gly
CA1705883
NM_001130978.2:c.1622A>G