Canonical Allele Identifier: PA2825767898
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 864337
ClinVar RCV Id: RCV001071496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Phe1398Ser
CA347228816
NM_001130985.2:c.4193T>C