Canonical Allele Identifier: PA2825134884
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 547704
ClinVar RCV Id: RCV000660131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Phe119del
CA645600895
NM_000268.4:c.357_359del