Canonical Allele Identifier: PA215753
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Glu328Val
CA021461
NM_000268.4:c.983A>T