Canonical Allele Identifier: PA658806659
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 500004
ClinVar RCV Id: RCV000598072 RCV000792953 RCV001535517 RCV003403397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Pro265Leu
CA1705463
NM_001130987.2:c.794C>T