Canonical Allele Identifier: PA2825135670
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1911532
ClinVar RCV Id: RCV002597022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Glu522Asp
CA411149800
NM_000268.4:c.1566G>C
CA411149801
NM_000268.4:c.1566G>T