Canonical Allele Identifier: PA645477568
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336950
ClinVar RCV Id: RCV000297254 RCV000392981 RCV000705827 RCV001828331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Ala457Val
CA1705708
NM_001130987.2:c.1370C>T