Allele Registry

Canonical Allele Identifier: PA658678072

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000540282

RCV000993215

ClinVar Variation:

470938

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Ile5011Val	CA7222963 NM_182914.2:c.15031A>G