Canonical Allele Identifier: PA161088
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134892
ClinVar RCV Id: RCV000121642 RCV000564583 RCV000733228 RCV001085689 RCV003398733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Asn36Ser
CA021291
NM_016418.5:c.107A>G