Allele Registry

Canonical Allele Identifier: PA645486485

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000326039

RCV001079812

RCV004021140

ClinVar Variation:

283619

HGVS (amino-acid)	Matching Registered Transcripts
NP_878918.2:p.Leu3105Phe	CA7221251 NM_182914.2:c.9315A>C CA389977928 NM_182914.2:c.9315A>T