Canonical Allele Identifier: PA645477701
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289963
ClinVar RCV Id: RCV001086957 RCV000726406 RCV001271534 RCV003910035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asn1369Ser
CA1706892
NM_001130987.2:c.4106A>G