Canonical Allele Identifier: PA2825767927
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501040
ClinVar RCV Id: RCV000658870 RCV001196059 RCV001140901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Val1421Ile
CA1706946
NM_001130985.2:c.4261G>A