Canonical Allele Identifier: PA645476990
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288625
ClinVar RCV Id: RCV000271058 RCV001855211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Thr75Met
CA1705259
NM_001130987.2:c.224C>T