Canonical Allele Identifier: PA2830393002
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 662489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Met519Ile
CA411149776
NM_181825.3:c.1557G>T
CA411149777
NM_181825.3:c.1557G>A
CA411149778
NM_181825.3:c.1557G>C