Allele Registry

Canonical Allele Identifier: PA2827402071

Gene: SYNE1 HGNC NCBI

ClinVar Allele:

207328

ClinVar RCV:

RCV000193297

RCV000291749

RCV000346757

RCV000951589

ClinVar Variation:

212341

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334630.1:p.Arg474Gln	CA206679 NM_001347701.2:c.1421G>A