Canonical Allele Identifier: PA915973861
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336964
ClinVar RCV Id: RCV000278825 RCV000373211 RCV001140034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Thr1068Ile
CA1706444
NM_001130982.2:c.3203C>T