Canonical Allele Identifier: PA645477685
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 196895
ClinVar RCV Id: RCV000177777 RCV000656846 RCV001084687 RCV001336578 RCV002516753 RCV003937609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Arg1272Trp
CA244680
NM_001130987.2:c.3814C>T