Canonical Allele Identifier: PA2830398785
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 457930
ClinVar RCV Id: RCV000533798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.His221Arg
CA411145642
NM_181830.3:c.662A>G