Canonical Allele Identifier: PA2573064559
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1300900
ClinVar RCV Id: RCV001733056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Arg192Trp
CA9393902
NM_001039876.3:c.574C>T