Canonical Allele Identifier: PA2830397588
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1911532
ClinVar RCV Id: RCV002597022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861967.1:p.Glu481Asp
CA411149800
NM_181829.3:c.1443G>C
CA411149801
NM_181829.3:c.1443G>T