Allele Registry

Canonical Allele Identifier: PA2825134964

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 426373

HGVS (amino-acid)	Matching Registered Transcripts
NP_000259.1:p.Phe162Leu	CA411142186 NM_000268.4:c.484T>C CA411142191 NM_000268.4:c.486T>A CA411142192 NM_000268.4:c.486T>G