Allele Registry

Canonical Allele Identifier: PA101871

Gene: NF2 HGNC NCBI

ClinVar RCV:

RCV000003458

ClinVar Variation:

3297

HGVS (amino-acid)	Matching Registered Transcripts
NP_000259.1:p.Phe62Ser	CA021406 NM_000268.4:c.185T>C