Canonical Allele Identifier: PA2825756239
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 500618
ClinVar RCV Id: RCV000592160 RCV000807941 RCV001276724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Ser454Thr
CA1705707
NM_001130980.2:c.1361G>C