Allele Registry

Canonical Allele Identifier: PA645486295

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 283981

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Asn385Ser	CA7219360 NM_182914.2:c.1154A>G