Canonical Allele Identifier: PA2829833614
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774430
ClinVar RCV Id: RCV002392432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Phe507Leu
CA411149689
NM_016418.5:c.1519T>C
CA411149693
NM_016418.5:c.1521C>A
CA411149694
NM_016418.5:c.1521C>G