Allele Registry

Canonical Allele Identifier: PA645486316

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000333138

RCV001087676

ClinVar Variation:

282271

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Asn889Asp	CA7219765 NM_182914.2:c.2665A>G