Canonical Allele Identifier: PA645395413
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 227088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Arg267Trp
CA9393853
NM_001039876.3:c.799C>T