Canonical Allele Identifier: PA2580135612
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2360822
ClinVar RCV Id: RCV004205651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Arg181Trp
CA9393910
NM_001039876.3:c.541C>T