Canonical Allele Identifier: PA645386587
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 426373
ClinVar RCV Id: RCV000489141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Phe162Leu
CA411142186
NM_016418.5:c.484T>C
CA411142191
NM_016418.5:c.486T>A
CA411142192
NM_016418.5:c.486T>G