Canonical Allele Identifier: PA2826845828
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2385081
ClinVar RCV Id: RCV004219925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284664.1:p.Val158Ala
CA9393849
NM_001297735.3:c.473T>C