Canonical Allele Identifier: PA2830392832
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 819284
ClinVar RCV Id: RCV001011703 RCV001759691 RCV001800918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Pro488Leu
CA411149572
NM_181825.3:c.1463C>T