Canonical Allele Identifier: PA2829466010
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 259085
ClinVar RCV Id: RCV000249294 RCV000532146 RCV000733997 RCV001833275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Val226Met
CA1705456
NM_003494.4:c.676G>A