Allele Registry

Canonical Allele Identifier: PA2830392942

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 1774430

HGVS (amino-acid)	Matching Registered Transcripts
NP_861546.1:p.Phe507Leu	CA411149689 NM_181825.3:c.1519T>C CA411149693 NM_181825.3:c.1521C>A CA411149694 NM_181825.3:c.1521C>G