Allele Registry

Canonical Allele Identifier: PA2829808658

Gene: SYNE2 HGNC NCBI

ClinVar Variation Id: 448621

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Ser3587Phe	CA7221607 NM_015180.5:c.10760C>T