Canonical Allele Identifier: PA916078844
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 403231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Ser497Thr
CA16609788
NM_181832.3:c.1490G>C