Canonical Allele Identifier: PA2830391536
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501455
ClinVar RCV Id: RCV002017480
ClinVar Variation Id: 2663242
ClinVar RCV Id: RCV003442430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Leu97Phe
CA411153229
NM_181825.3:c.291G>C
CA411153231
NM_181825.3:c.291G>T