Allele Registry

Canonical Allele Identifier: PA2829807069

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000176597

RCV001087661

ClinVar Variation:

195914

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Thr1079Ala	CA242588 NM_015180.5:c.3235A>G