Canonical Allele Identifier: PA2830392795
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903628
ClinVar RCV Id: RCV002586500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Lys478Arg
CA411149189
NM_181825.3:c.1433A>G