Canonical Allele Identifier: PA2825696021
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471324
ClinVar RCV Id: RCV000533199 RCV001834801 RCV001755866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Arg2045Trp
CA1707654
NM_001130455.2:c.6133C>T