Canonical Allele Identifier: PA2825766949
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 813959
ClinVar RCV Id: RCV001004943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Cys539Arg
CA347217368
NM_001130985.2:c.1615T>C