Allele Registry

Canonical Allele Identifier: PA658677866

Gene: SYNE2 HGNC NCBI

ClinVar Allele:

441657

ClinVar RCV:

RCV000516240

RCV000705421

ClinVar Variation:

448633

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Met1719Val	CA7220413 NM_182914.2:c.5155A>G