Allele Registry

Canonical Allele Identifier: PA645486541

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000699066

RCV001288052

RCV004021591

ClinVar Variation:

313577

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Thr4205Ile	CA7222222 NM_182914.2:c.12614C>T