Canonical Allele Identifier: PA645477776
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288577
ClinVar RCV Id: RCV000647992 RCV000726189 RCV001271547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asn1635Ser
CA1707164
NM_001130987.2:c.4904A>G