Canonical Allele Identifier: PA2830401955
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_861969.1:p.Lys395Arg
CA411149189
NM_181831.3:c.1184A>G