Canonical Allele Identifier: PA645477543
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94365
ClinVar RCV Id: RCV000080333 RCV000696449 RCV001831823 RCV003330426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val318Glu
CA222220
NM_001130987.2:c.953T>A