Allele Registry

Canonical Allele Identifier: PA239952

Gene: SYNE1 HGNC NCBI

ClinVar RCV:

RCV000174412

RCV001237264

ClinVar Variation:

194125

HGVS (amino-acid)	Matching Registered Transcripts
NP_892006.3:p.Trp326Arg	CA239951 NM_182961.4:c.976T>C CA366144521 NM_182961.4:c.976T>A