Canonical Allele Identifier: PA2825135390
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Thr380Ala
CA411147991
NM_000268.4:c.1138A>G