Allele Registry

Canonical Allele Identifier: PA2830397535

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 1774430

HGVS (amino-acid)	Matching Registered Transcripts
NP_861967.1:p.Phe466Leu	CA411149689 NM_181829.3:c.1396T>C CA411149693 NM_181829.3:c.1398C>A CA411149694 NM_181829.3:c.1398C>G