Allele Registry

Canonical Allele Identifier: PA101751

Gene: NF2 HGNC NCBI

ClinVar RCV:

RCV000003448

ClinVar Variation:

3287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000259.1:p.Gln538Pro	CA021363 NM_000268.4:c.1613A>C