Canonical Allele Identifier: PA2825771798
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1984899
ClinVar RCV Id: RCV002775735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val1377Ile
CA1706899
NM_001130987.2:c.4129G>A