Canonical Allele Identifier: PA2580550180
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774430
ClinVar RCV Id: RCV002392432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Phe507Leu
CA411149689
NM_181832.3:c.1519T>C
CA411149693
NM_181832.3:c.1521C>A
CA411149694
NM_181832.3:c.1521C>G