Canonical Allele Identifier: PA916078814
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 457893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Val430Leu
CA411148502
NM_181832.3:c.1288G>C
CA411148504
NM_181832.3:c.1288G>T