Canonical Allele Identifier: PA2825135592
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773078
ClinVar RCV Id: RCV002394734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Pro486Leu
CA411149558
NM_000268.4:c.1457C>T