Canonical Allele Identifier: PA2830399739
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2677249
ClinVar RCV Id: RCV003463180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Leu456Val
CA411150081
NM_181830.3:c.1366C>G