Canonical Allele Identifier: PA645386698
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 403231
ClinVar RCV Id: RCV000455655 RCV000804584 RCV001011871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Ser497Thr
CA16609788
NM_016418.5:c.1490G>C