Canonical Allele Identifier: PA2830392014
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757311
ClinVar RCV Id: RCV002378343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Ala238Ser
CA411143801
NM_181825.3:c.712G>T