Allele Registry

Canonical Allele Identifier: PA645486490

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV001061448

ClinVar Variation:

313546

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Lys3135Arg	CA7221263 NM_182914.2:c.9404A>G