Canonical Allele Identifier: PA2825746988
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538634
ClinVar RCV Id: RCV000648001 RCV001004972 RCV001563954 RCV001563955 RCV001756080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Asn263Ser
CA1705487
NM_001130976.2:c.788A>G