Allele Registry

Canonical Allele Identifier: PA645486625

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000528583

RCV000993217

ClinVar Variation:

313637

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Ala6064Thr	CA7223961 NM_182914.2:c.18190G>A