Allele Registry

Canonical Allele Identifier: PA2829808988

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000330788

ClinVar Variation:

313567

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Gln4051Glu	CA7222029 NM_015180.5:c.12151C>G