Canonical Allele Identifier: PA2830393038
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2135982
ClinVar RCV Id: RCV003059830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Lys531Asn
CA411150029
NM_181825.3:c.1593G>C
CA411150030
NM_181825.3:c.1593G>T