Canonical Allele Identifier: PA2830396581
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713613
ClinVar RCV Id: RCV003501347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861967.1:p.Phe266Leu
CA411145695
NM_181829.3:c.796T>C
CA411145712
NM_181829.3:c.798T>A
CA411145714
NM_181829.3:c.798T>G