Allele Registry

Canonical Allele Identifier: PA2829810684

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 313663

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Ser6785Leu	CA7224861 NM_015180.5:c.20354C>T