Canonical Allele Identifier: PA915973848
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 652065
ClinVar RCV Id: RCV000807552 RCV001825604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Pro1051Leu
CA1706429
NM_001130982.2:c.3152C>T