Canonical Allele Identifier: PA2825135704
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2677249
ClinVar RCV Id: RCV003463180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Leu539Val
CA411150081
NM_000268.4:c.1615C>G