Allele Registry

Canonical Allele Identifier: PA2830399741

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 565467

HGVS (amino-acid)	Matching Registered Transcripts
NP_861968.1:p.Asn457Ser	CA032390 NM_181830.3:c.1370A>G