Canonical Allele Identifier: PA2830399170
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 527695
ClinVar RCV Id: RCV001249076 RCV001198705 RCV000632640 RCV000765629 RCV001010465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Arg328His
CA037304
NM_181830.3:c.983G>A