Canonical Allele Identifier: PA2826845832
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 227091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284664.1:p.Gln165His
CA9393840
NM_001297735.3:c.495G>C
CA405431520
NM_001297735.3:c.495G>T