Canonical Allele Identifier: PA2829833489
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2123079
ClinVar RCV Id: RCV003054900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Glu474Asp
CA411149151
NM_016418.5:c.1422G>C
CA411149153
NM_016418.5:c.1422G>T