Canonical Allele Identifier: PA2830399698
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 854568
ClinVar RCV Id: RCV001059647 RCV004031891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.His451Tyr
CA032373
NM_181830.3:c.1351C>T