Canonical Allele Identifier: PA2825135238
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713613
ClinVar RCV Id: RCV003501347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Phe307Leu
CA411145695
NM_000268.4:c.919T>C
CA411145712
NM_000268.4:c.921T>A
CA411145714
NM_000268.4:c.921T>G