Allele Registry

Canonical Allele Identifier: PA2742019448

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 2713613

HGVS (amino-acid)	Matching Registered Transcripts
NP_861970.1:p.Phe307Leu	CA411145695 NM_181832.3:c.919T>C CA411145712 NM_181832.3:c.921T>A CA411145714 NM_181832.3:c.921T>G