Canonical Allele Identifier: PA2742019448
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713613
ClinVar RCV Id: RCV003501347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Phe307Leu
CA411145695
NM_181832.3:c.919T>C
CA411145712
NM_181832.3:c.921T>A
CA411145714
NM_181832.3:c.921T>G