Allele Registry

Canonical Allele Identifier: PA2830422388

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 313663

HGVS (amino-acid)	Matching Registered Transcripts
NP_878917.1:p.Ser456Leu	CA7224861 NM_182913.2:c.1367C>T