Allele Registry

Canonical Allele Identifier: PA2830422073

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 313670

HGVS (amino-acid)	Matching Registered Transcripts
NP_878914.1:p.Thr423Asn	CA7224998 NM_182910.2:c.1268C>A