Allele Registry

Canonical Allele Identifier: PA1139746597

Gene: NF2 HGNC NCBI

ClinVar RCV:

RCV001049541

ClinVar Variation:

846276

HGVS (amino-acid)	Matching Registered Transcripts
NP_861970.1:p.Gln324Glu	CA411146013 NM_181832.3:c.970C>G