Allele Registry

Canonical Allele Identifier: PA2829806986

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000333138

RCV001087676

ClinVar Variation:

282271

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Asn889Asp	CA7219765 NM_015180.5:c.2665A>G