Canonical Allele Identifier: PA913200019
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 594211
ClinVar RCV Id: RCV000729447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Val232Ala
CA9393866
NM_001039876.3:c.695T>C