Canonical Allele Identifier: PA2829866180
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721051
ClinVar RCV Id: RCV002294771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Leu299Val
CA411145572
NM_016418.5:c.895C>G