Canonical Allele Identifier: PA2830397606
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231081
ClinVar RCV Id: RCV004523195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861967.1:p.Tyr487Cys
CA411150003
NM_181829.3:c.1460A>G