Canonical Allele Identifier: PA2825135567
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2123079
ClinVar RCV Id: RCV003054900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Glu474Asp
CA411149151
NM_000268.4:c.1422G>C
CA411149153
NM_000268.4:c.1422G>T