Canonical Allele Identifier: PA2825135571
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719798
ClinVar RCV Id: RCV002303983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Ala476Thr
CA411149168
NM_000268.4:c.1426G>A