Allele Registry

Canonical Allele Identifier: PA645486608

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 282879

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Pro5531Thr	CA7223415 NM_182914.2:c.16591C>A