Canonical Allele Identifier: PA2830397381
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514091
ClinVar RCV Id: RCV002018564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861967.1:p.Leu431Phe
CA411149127
NM_181829.3:c.1291C>T