Canonical Allele Identifier: PA2825751021
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289244
ClinVar RCV Id: RCV000285614 RCV000647999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Cys1891Phe
CA10606384
NM_001130977.2:c.5672G>T