Canonical Allele Identifier: PA2825134818
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1017607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Leu82Pro
CA411152973
NM_000268.4:c.245T>C