Canonical Allele Identifier: PA2830393011
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1911532
ClinVar RCV Id: RCV002597022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Glu522Asp
CA411149800
NM_181825.3:c.1566G>C
CA411149801
NM_181825.3:c.1566G>T