Allele Registry

Canonical Allele Identifier: PA645486390

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000340242

RCV000812641

ClinVar Variation:

281151

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Ala1665Val	CA7220363 NM_182914.2:c.4994C>T