Canonical Allele Identifier: PA2830393670
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368584
ClinVar RCV Id: RCV001867567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.Tyr111Cys
CA411142128
NM_181828.3:c.332A>G